Haplogroup O-M122 Explained

O-M122
Origin-Date:33,943 (95% CI 25,124 <-> 37,631) ybp [1]

35,000 (with slower average mutation rate) or 30,000 (with faster average mutation rate) years ago
Tmrca:30,365 (95% CI 22,492 <-> 33,956) ybp
Ancestor:O-M175
Mutations:M122 [2]
Members:Nyishi 94%, Adi 89%, Tamang 87%, Kachari (Boro) 85%,[3] Apatani 82%, Rabha 76.5%, Naga 76%, Bhutanese 74%, Naiman Kazakhs 68%, Han Chinese 56%, Tibetan 48%, She People 48% (78.6% Northern, 62.7%), Manchus 47%, Hmong/Miao 46% (69.0% China, 64.3% Thailand, 44.0% Hunan, 41.2% Laos, 36.7% Yunnan, 30.6% Guizhou, 14.6% Điện Biên Phủ), Vietnamese 44%, Korean 43%, Karen 37%,[4] Filipinos 33%, Southwestern Tai approx. 30.4% (Shan 40%, Siamese 39.5%, Northern Thai 37.2%, Yong 37%, Tai Lue 29%, Saek 29%, Phuan 29%, Thái in Vietnam 29%, Lao 27.5%, Kaleun 24%, Nyaw 22%, Isan 21%, Tai Khün 21%, Phutai 17%, Tai Dam 14%)

Haplogroup O-M122 (also known as Haplogroup O2 (formerly Haplogroup O3)) is an Eastern Eurasian Y-chromosome haplogroup. The lineage ranges across Southeast Asia and East Asia, where it dominates the paternal lineages with extremely high frequencies. It is also significantly present in Central Asia, especially among the Naiman tribe of Kazakhs.

This lineage is a descendant haplogroup of haplogroup O-M175.

Origins

Researchers believe that O-M122 first appeared in Southeast Asia approximately 25,000-30,000 years ago, or roughly between 30,000 and 35,000 years ago according to more recent studies.[5] In a systematic sampling and genetic screening of an East Asian–specific Y-chromosome haplogroup (O-M122) in 2,332 individuals from diverse East Asian populations, results indicate that the O-M122 lineage is dominant in East Asian populations, with an average frequency of 44.3%. Microsatellite data show that the O-M122 haplotypes are more diverse in Southeast Asia than those in northern East Asia. This suggests a southern origin of the O-M122 mutation to be likely.

It was part of the settlement of East Asia. However, the prehistoric peopling of East Asia by modern humans remains controversial with respect to early population migrations and the place of the O-M122 lineage in these migrations is ambivalent.

Distribution

Although Haplogroup O-M122 appears to be primarily associated with ethnic Tibeto-Burman speaking groups inhabiting the Seven Sister States of north eastern India, it also forms a significant component of the Y-chromosome diversity of most modern populations of the East Asian region.

East Asia

Haplogroup O-M122 is found in approximately 53.27% of all modern Chinese males[6] (with frequency ranging from 30/101=29.7% among Pinghua-speaking Hans in Guangxi to 110/148=74.3% among Hans in Changting, Fujian), about 40% of Manchu, Chinese Mongolian, Korean, and Vietnamese males, about 33.3% to 62% of Filipino males, about 10.5% to 55.6% of Malaysian males, about 10% (4/39 Guide County, Qinghai) to 45% (22/49 Zhongdian County, Yunnan) of Tibetan males, about 20% (10/50 Shuangbai, northern Yunnan) to 44% (8/18 Xishuangbanna, southern Yunnan) of Yi males, about 25% of Zhuang and Indonesian males, and about 16% to 20% of Japanese males. The distribution of Haplogroup O-M122 stretches far into Asia (approx. 40% of Dungans, 30% of Salars, 28% of Bonan, 24% of Dongxiang, 18% to 22.8% of Mongolian citizens in Ulaanbaatar, 11%-15.4% of Khalkha Mongolians, but also as high as 31.1%, 12% of Uyghurs, 9% of Kazakhs, but in the Naiman of Kazakhs 65.81%, 6.8% of Kalmyks (17.1% of Khoshuud, 6.1% of Dörwöd, 3.3% of Torguud, 0% of Buzawa), 6.2% of Altaians, 5.3% of Kyrgyz, 4.1% of Uzbeks, and 4.0% of Buryats.

Modern northern Han Chinese Y haplogroups and mtdna match those of ancient northern Han Chinese ancestors 3,000 years ago from the Hengbei archeological site. 89 ancient samples were taken. Y haplogroups O3a, O3a3, M, O2a, Q1a1, and O* were all found in Hengbei samples.[7] Three men who lived in the Neolithic era are the ancestors of 40% of Han Chinese, with their Y haplogroups being subclades of O3a-M324 and they are estimated to have lived 6,800 years ago, 6,500 years ago and 5,400 years ago.[8]

The East Asian O3-M122 Y chromosome Haplogroup is found in large quantities in other Muslims close to the Hui people like Dongxiang, Bo'an and Salar. The majority of Tibeto-Burmans, Han Chinese, and Ningxia and Liaoning Hui share paternal Y chromosomes of East Asian origin which are unrelated to Middle Easterners and Europeans. In contrast to distant Middle Eastern and Europeans whom the Muslims of China are not related to, East Asians, Han Chinese, and most of the Hui and Dongxiang of Linxia share more genes with each other. This indicates that native East Asian populations converted to Islam and were culturally assimilated to these ethnicities and that Chinese Muslim populations are mostly not descendants of foreigners as claimed by some accounts while only a small minority of them are.[9]

South Asia

Haplogroup O-M122 is restricted among tribal groups of Northeast India where it is found at very high frequencies. In Arunachal Pradesh, it is found at 89% among Adi, 82% among Apatani, and 94% among Nishi, while the Naga people show it at 100%. In Meghalaya, 59.2% (42/71) of a sample of Garos and 31.7% (112/353) of a sample of Khasis have been found to belong to O-M122. In Nepal, Tamang people present a very high frequency of O-M122 (39/45 = 86.7%), while much lower percentages of Newar (14/66 = 21.2%) and the general population of Kathmandu (16/77 = 20.8%) belong to this haplogroup. A study published in 2009 found O-M122 in 52.6% (30/57, including 28 members of O-M117 and two members of O-M134(xM117)) of a sample of Tharus from a village in Chitwan District of south-central Nepal, 28.6% (22/77, all O-M117) of a sample of Tharus from another village in Chitwan District, and 18.9% (7/37, all O-M117) of a sample of Tharus from a village in Morang District of southeastern Nepal. In contrast, the same study found O-M122 in only one individual in a sample of non-Tharu Hindus collected in Chitwan District (1/26 = 3.8% O-M134(xM117)), one tribal individual from Andhra Pradesh, India (1/29 = 3.4% O-M117), and one individual in a sample of Hindus from New Delhi, India (1/49 = 2.0% O-M122(xM134)).

Southeast Asia

Among all the populations of East and Southeast Asia, Haplogroup O-M122 is most closely associated with those that speak a Sinitic, Tibeto-Burman, or Hmong–Mien language. Haplogroup O-M122 comprises about 50% or more of the total Y-chromosome variation among the populations of each of these language families. The Sinitic and Tibeto-Burman language families are generally believed to be derived from a common Sino-Tibetan protolanguage, and most linguists place the homeland of the Sino-Tibetan language family somewhere in northern China. The Hmong–Mien languages and cultures, for various archaeological and ethnohistorical reasons, are also generally believed to have derived from a source somewhere north of their current distribution, perhaps in northern or central China. The Tibetans, however, despite the fact that they speak a language of the Tibeto-Burman language family, have high percentages of the otherwise rare haplogroups D-M15 and D3, which are also found at much lower frequencies among the members of some other ethnic groups in East Asia and Central Asia.

Haplogroup O-M122 has been implicated as a diagnostic genetic marker[10] of the Austronesian expansion when it is found in populations of insular Southeast Asia and Oceania. It appears at moderately high frequencies in the Philippines, Malaysia, and Indonesia. Its distribution in Oceania is mostly limited to the traditionally Austronesian culture zones, chiefly Polynesia (approx. 25% to 32.5%). O-M122 is found at generally lower frequencies in coastal and island Melanesia, Micronesia, and Taiwanese aboriginal tribes (18% to 27.4% of Micronesians), and 5% of Melanesians, albeit with reduced frequencies of most subclades.

Haplogroup O-M122 Y-chromosomes, which are not defined by any identified downstream markers, are actually more common among certain non-Han Chinese populations than among Han Chinese ones, and the presence of these O-M122* Y-chromosomes among various populations of Central Asia, East Asia, and Oceania is more likely to reflect a very ancient shared ancestry of these populations rather than the result of any historical events. It remains to be seen whether Haplogroup O-M122* Y-chromosomes can be parsed into distinct subclades that display significant geographical or ethnic correlations.

Subclade Distribution

Paragroup O-M122*

Paragroup O2*-M122(xO2a-P197) Y-DNA is quite rare, having been detected only in 2/165 = 1.2% of a sample of Han Chinese in a pool of samples from mainland China, Taiwan, the Philippines, Vietnam, and Malaysia (n=581), 8/641 = 1.2% of a sample of Balinese in a pool of samples from western Indonesia (n=960), and 7/350 = 2.0% of a sample of males from Sumba in a pool of samples from eastern Indonesia (n=957). In the same study, O2*-M122(xO2a-P197) Y-DNA was not observed in a pool of samples from Oceania (n=182).

In 2005, Chinese researchers published a paper reporting the detection of O2*-M122(xO2a-M324) Y-DNA in 1.6% (8/488) of a pool of seven samples of Han Chinese (3/64 = 4.7% Sichuan, 2/98 = 2.0% Zibo, Shandong, 1/60 = 1.7% Inner Mongolia, 1/81 = 1.2% Yunnan, 1/86 = 1.2% Laizhou, Shandong, 0/39 Guangxi, 0/60 Gansu). O2*-M122(xO2a-M324) Y-DNA also was detected in the following samples of ethnic minorities in China: 5.9% (1/17) Jingpo from Yunnan, 4.3% (2/47) Zhuang from Yunnan, 4.1% (2/49) Lisu from Yunnan, 3.2% (1/31) Wa from Yunnan, 2.6% (1/39) Zhuang from Guangxi, 2.5% (2/80) Bai from Yunnan, 2.4% (1/41) Hani from Yunnan, 2.3% (2/88) Lahu from Yunnan, 2.1% (1/47) Yi from Yunnan, 2.1% (1/48) Miao from Yunnan, 1.5% (2/132) Dai from Yunnan, 1.0% (1/105) Miao from Hunan, and 0.9% (2/225) Yao from Guangxi.[11]

O2*-M122(xO2a-M324) Y-DNA has been found as a singleton (1/156 = 0.6%) in a sample from Tibet. It also has been found as a singleton in a sample of nineteen members of the Chin people in Chin State, Myanmar.[12]

In a paper published in 2011, Korean researchers have reported finding O2*-M122(xO2a-M324) Y-DNA in the following samples: 5.9% (3/51) Beijing Han, 3.1% (2/64) Filipino, 2.1% (1/48) Vietnamese, 1.7% (1/60) Yunnan Han, 0.4% (2/506) Korean, including 1/87 from Jeju and 1/110 from Seoul-Gyeonggi. In another study published in 2012, Korean researchers have found O-M122(xM324) Y-DNA in 0.35% (2/573) of a sample from Seoul; however, no individual belonging to O-M122(xM324) was observed in a sample of 133 individuals from Daejeon.

In 2011, Chinese researchers published a paper reporting their finding of O2*-M122(xO2a-M324) Y-DNA in 3.0% (5/167) of a sample of Han Chinese with origins in East China (defined as consisting of Jiangsu, Zhejiang, Shanghai, and Anhui) and in 1.5% (1/65) of a sample of Han Chinese with origins in Southern China. O2* Y-DNA was not detected in their sample of Han Chinese with origins in Northern China (n=129).

In a paper published in 2012, O2*-M122(xO2a-P200) Y-DNA was found in 12% (3/25) of a sample of Lao males from Luang Prabang, Laos. O2* Y-DNA was not detected in this study's samples of Cham from Binh Thuan, Vietnam (n=59), Kinh from Hanoi, Vietnam (n=76), or Thai from northern Thailand (n=17).

Trejaut et al. (2014) found O2-M122(xO2a-M324) in 6/40 (15.0%) Siraya in Kaohsiung, 1/17 (5.9%) Sulawesi, 1/25 (4.0%) Paiwan, 2/55 (3.6%) Fujian Han, 1/30 (3.3%) Ketagalan, 2/60 (3.3%) Taiwan Minnan, 1/34 (2.9%) Taiwan Hakka, 1/38 (2.6%) Siraya in Hwalien, 5/258 (1.9%) miscellaneous Han volunteers in Taiwan, and 1/75 (1.3%) in a sample of the general population of Thailand.

Brunelli et al. (2017) found O2-M122(xO2a-M324) in 5/66 (7.6%) Tai Yuan, 1/91 (1.1%) Tai Lue, and 1/205 (0.5%) Khon Mueang in samples of the people of Northern Thailand.

O-M324

O-M121

O2a1a1a1a1-M121 is a subclade of O2a1-L127.1, parallel to O2a1b-M164 and O2a1c-JST002611.

In an early survey of Y-DNA variation in present-day human populations of the world, O-M121 was detected only in 5.6% (1/18) of a sample from Cambodia and Laos and in 5.0% (1/20) of a sample from China.

In a large study of 2,332 unrelated male samples collected from 40 populations in East Asia (and especially Southwest China), O-M121/DYS257 Y-DNA was detected only in 7.1% (1/14) of a sample of Cambodians and in 1.0% (1/98) of a sample of Han Chinese from Zibo, Shandong.

In a study published in 2011, O-M121 Y-DNA was found in 1.2% (2/167) of a sample of Han Chinese with origins in East China, defined as consisting of Jiangsu, Anhui, Zhejiang, and Shanghai, and in 0.8% (1/129) of a sample of Han Chinese with origins in Northern China. O-M121 was not detected in this study's sample of Han Chinese with origins in Southern China (n=65).

O-L599 (considered to be phylogenetically equivalent to O-M121[13]) also has been found in one individual in the 1000 Genomes Project sample of Han Chinese from Hunan, China (n=37), one individual in the 1000 Genomes Project sample of Kinh from Ho Chi Minh City, Vietnam, one individual in the Human Genome Diversity Project sample of Tujia, an individual from Singapore, and an individual from the Jakarta metropolitan area. According to 23魔方, O-L599 currently accounts for about 0.79% of the male population in China and is concentrated in Fujian, Taiwan, Jiangxi, Anhui, Hubei, Zhejiang and other provinces and cities; it appears to have undergone explosive population growth between about 2600 and 2300 years ago.

O-M164

O2a1b-M164 is a subclade of O2a1-L127.1, parallel to O2a1a1a1a1-M121 and O2a1c-JST002611. In an early survey of Y-DNA variation in present-day human populations of the world, O-M164 was detected only in 5.6% (1/18) of a sample from Cambodia and Laos.

In a large study of 2,332 unrelated male samples collected from 40 populations in East Asia (and especially Southwest China), O2a1b-M164 Y-DNA was detected only in 7.1% (1/14) of a sample of Cambodians.

According to 23魔方, O-M164 is a recent branch (TMRCA 2120 years) downstream of O2a1c-JST002611 rather than parallel to it. Out of fourteen members total, six are from Guangdong, five are from Fujian, one is from Nantong, one is from Wenzhou, and one is from Taiwan.[14]

O-JST002611

Haplogroup O2a1c-JST002611 is derived from O2-M122 via O2a-M324/P93/P197/P199/P200 and O2a1-L127.1/L465/L467. O2a1c-JST002611 is the most commonly observed type of O2a1 Y-DNA, and, more generally, represents the majority of extant O2-M122 Y-DNA that does not belong to the expansive subclade O2a2-P201. Haplogroup O2a1c-JST002611 was first identified in 3.8% (10/263) of a sample of Japanese. It also has been found in 3.5% (2/57) of the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project, including one member of the rare and deeply divergent paragroup O2a1c1-F18*(xO2a1c1a1-F117, O2a1c1a2-F449).[15] Subsequently, this haplogroup has been found with higher frequency in some samples taken in and around China, including 12/58 = 20.7% Miao (China), 10/70 = 14.3% Vietnam, 18/165 = 10.9% Han (China & Taiwan), 4/49 = 8.2% Tujia (China). O-002611 also has been found in a singleton from the Philippines (1/48 = 2.1%), but it has not been detected in samples from Malaysia (0/32), Taiwanese Aboriginals (0/48), She from China (0/51), Yao from China (0/60), Oceania (0/182), eastern Indonesia (0/957), or western Indonesia (0/960). Haplogroup O2a1c‐JST002611 is prevalent in different ethnic groups in China and Southeast Asia, including Vietnam (14.29%), Sichuan of southwestern China (Han, 14.60%; Tibetan in Xinlong County, 15.22%),[16] Jilin of northeastern China (Korean, 9.36%), Inner Mongolia (Mongolian, 6.58%), and Gansu of northwestern China (Baima, 7.35%; Han, 11.30%).[17] Y-DNA belonging to haplogroup O-JST002611 has been observed in 10.6% (61/573) of a sample collected in Seoul and 8.3% (11/133) of a sample collected in Daejeon, South Korea.[18]

According to 23魔方, haplogroup O-IMS-JST002611 currently accounts for approximately 14.72% of the entire male population of China, and its TMRCA is estimated to be 13,590 years.[19] Yan et al. (2011) have found O-IMS-JST002611 in 16.9% (61/361) of a pool of samples of Han Chinese from East China (n=167), North China (n=129), and South China (n=65). According to Table S4 of He Guanglin et al. 2023, haplogroup O2a1b-IMS-JST002611 has been found in 17.50% (366/2091) of a pool of samples of Han Chinese from various provinces and cities of China.[20] Haplogroup O2a1b-IMS-JST002611 is the second most common Y-DNA haplogroup among Han Chinese (and among Chinese in general) after haplogroup O2a2b1a1-M117.

O-P201

O2a2-JST021354/P201 has been divided into primary subclades O2a2a-M188 (TMRCA 18,830 ybp, accounts for approximately 4.74% of all males in present-day China[21]) and O2a2b-P164 (TMRCA 20,410 ybp, accounts for approximately 30.4% of all males in present-day China[22] [23]). Among the various branches of O2a2a-M188, O-M7 (TMRCA 14,510 ybp, accounts for approximately 2.15% of all males in present-day China[24]) is notable for its relatively high frequency over a wide swath of Southeast Asia and southern China, especially among certain populations that currently speak Hmong-Mien, Austroasiatic, or Austronesian languages. Other branches of O2a2a-M188, such as O-CTS201 (TMRCA 16,070 ybp, accounts for approximately 1.76% of all males in present-day China[25]), O-MF39662 i.e. O-F2588(xCTS445), and O-MF109044 i.e. O-M188(xF2588) (TMRCA 9,690 ybp, accounts for approximately 0.4% of all males in present-day China[26]) have been found with generally low frequency in China; however, the O-CTS201 > O-FGC50590 > O-MF114497 subclade is fairly common among males in Korea and Japan. O2a2b-P164 has been divided cleanly into O2a2b1-M134 (TMRCA 17,450 ybp, accounts for approximately 27.58% of all males in present-day China[27]), which has been found with high frequency throughout East Asia and especially among speakers of Sino-Tibetan languages, and O2a2b2-AM01822 (TMRCA 16,000 ybp, accounts for approximately 2.80% of all males in present-day China[28]), which has been found with relatively low frequency but high diversity throughout East Asia and with high frequency in Austronesia.

O2a2-P201(xO2a2a1a2-M7, O2a2b1-M134) Y-DNA has been detected with high frequency in many samples of Austronesian-speaking populations, in particular some samples of Batak Toba from Sumatra (21/38 = 55.3%), Tongans (5/12 = 41.7%), and Filipinos (12/48 = 25.0%). Outside of Austronesia, O2a2-P201(xO2a2a1a2-M7, O2a2b1-M134) Y-DNA has been observed in samples of Tujia (7/49 = 14.3%), Han Chinese (14/165 = 8.5%), Japanese (11/263 = 4.2%), Miao (1/58 = 1.7%), and Vietnam (1/70 = 1.4%).

O-M159

O2a2a1a1a-M159 is a subclade of O2a2-P201 and O2a2a1a1-CTS201. In an early survey of Y-DNA variation in present-day human populations of the world, O-M159 was detected only in 5.0% (1/20) of a sample from China.

According to 23魔方, the TMRCA of haplogroup O-M159 is estimated to be 8,870 years. It is currently distributed mainly in southern China, and it is estimated to account for about 0.79% of the total male population of China.[29]

Unlike its phylogenetic siblings, O-M7 and O-M134, O-M159 is very rare, having been found only in 2.9% (1/35) of a sample of Han males from Meixian, Guangdong in a study of 988 males from East Asia.

In a study published in 2011, O-M159 was detected in 1.5% (1/65) of a sample of Han Chinese with origins in Southern China. O-M159 was not detected in the same study's samples of Han Chinese with origins in East China (n=167) or Northern China (n=129).

Trejaut et al. (2014) found O-M159 in 5.0% (3/60) Minnan in Taiwan, 4.2% (1/24) Hanoi, Vietnam, 3.88% (10/258) miscellaneous Han volunteers in Taiwan, 3.6% (2/55) Han in Fujian, 3.24% (12/370) Plains Aborigines in Taiwan (mostly assimilated to Han Chinese), 1.04% (2/192) Western Indonesia (1/25 Kalimantan, 1/26 Sumatra), and 0.68% (1/146) Philippines (1/55 South Luzon).

Kutanan et al. (2019) found O-M159 in 1.6% (2/129) of their samples of Thai people from Central Thailand.

O-M7

Haplogroup O2a2a1a2-M7 Y-DNA has been detected with high frequency in some samples of populations who speak Hmong-Mien languages, Katuic languages, or Bahnaric languages, scattered through some mostly mountainous areas of southern China, Laos, and Vietnam.

O-M7 has been noted for having a widespread but uneven distribution among populations that speak Hmong-Mien languages, such as She (29/51 = 56.9% She, 10/34 = 29.4% She, 14/56 = 25.0% Northern She from Zhejiang), Miao (21/58 = 36.2% Miao from China, 17/51 = 33.3% Hmong Daw from northern Laos, 6/49 = 12.2% Yunnan Miao, 2/49 = 4.1% Guizhou Miao, 4/100 = 4.0% Hunan Miao), and Yao (18/35 = 51.4% Yao from Liannan, Guangdong, 29/60 = 48.3% Yao from Guangxi, 12/35 = 34.3% Yao from Bama, Guangxi, 12/37 = 32.4% Zaomin from Guangdong, 5/36 = 13.9% Bunu from Guangxi, 1/11 = 9.1% Top-Board Mien, 3/41 = 7.3% Native Mien, 2/31 = 6.5% Southern Mien from Guangxi, 1/19 = 5.3% Flowery-Headed Mien from Guangxi, 1/20 = 5.0% Mountain Straggler Mien from Hunan, 1/28 = 3.6% Blue Kimmun from Guangxi, 1/31 = 3.2% Pahng from Guangxi, 1/47 = 2.1% Western Mien from Yunnan, 0/11 Thin Board Mien, 0/31 Lowland Yao from Guangxi, 0/32 Mountain Kimmun from Yunnan, 0/33 Northern Mien, and 0/41 Lowland Kimmun from Guangxi).

Cai et al. (2011) have reported finding high frequencies of O-M7 in their samples of Katuic (17/35 = 48.6% Ngeq, 10/45 = 22.2% Katu, 6/37 = 16.2% Kataang, 3/34 = 8.8% Inh (Ir), 4/50 = 8.0% So, 1/39 = 2.6% Suy) and Bahnaric (15/32 = 46.9% Jeh, 17/50 = 34.0% Oy, 8/32 = 25.0% Brau, 8/35 = 22.9% Talieng, 4/30 = 13.3% Alak, 6/50 = 12.0% Laven) peoples from southern Laos. However, O-M7 has been found only with low frequency in samples of linguistically related Khmuic populations from northern Laos (1/50 = 2.0% Mal, 1/51 = 2.0% Khmu, 0/28 Bit, 0/29 Xinhmul), Vietic peoples from Vietnam and central Laos (8/76 = 10.5% Kinh from Hanoi, Vietnam, 4/50 = 8.0% Kinh from northern Vietnam,[30] 2/28 = 7.1% Bo, 4/70 = 5.7% Vietnamese, 0/12 Muong, 0/15 Kinh, 0/38 Aheu), Palaungic peoples from northwestern Laos and southwestern Yunnan (2/35 = 5.7% Lamet, 0/29 Ava, 0/52 Blang), and Pakanic peoples from southeastern Yunnan and northwestern Guangxi (0/30 Palyu, 0/32 Bugan).

Haplogroup O-M7 has been found with notable frequency in some samples of Austronesian populations from the central part of the Malay Archipelago (17/86 = 19.8% Indonesians from Borneo, 4/32 = 12.5% Malaysia, 7/61 = 11.5% Java (mostly sampled in Dieng), 6/56 = 10.7% Sumatra, 4/53 = 7.5% Java, 1/17 = 5.9% Malaysia), but the frequency of this haplogroup appears to drop off very quickly toward the east (1/48 = 2.1% Philippines, 5/641 = 0.8% Balinese, 0/9 Timor, 0/28 Alor, 0/30 Moluccas, 0/31 Nusa Tenggaras, 0/33 Moluccas, 0/37 Philippines, 0/40 Borneo, 0/48 Taiwanese Aboriginals, 0/54 Mandar from Sulawesi, 0/92 Lembata, 0/350 Sumba, 0/394 Flores) and toward the west (0/38 Batak Toba from Sumatra, 0/60 Nias, 0/74 Mentawai). O-M7 has been found in 14.8% (4/27) of a sample of Giarai from southern Vietnam, 8.3% (2/24) of a sample of Ede from southern Vietnam, and 5.1% (3/59) of a sample of Cham from Binh Thuan, Vietnam. These Chamic-speaking peoples inhabit southern Vietnam and eastern Cambodia, but their languages are related to those of the Acehnese and Malays. O-M7 also has been found in 21.1% (8/38) of a small set of samples of highlanders of northern Luzon (including 1/1 Ifugao, 1/2 Ibaloi, 4/12 Kalangoya, and 2/6 Kankanaey).[31]

In the northern fringes of its distribution, O-M7 has been found in samples of Oroqen (2/31 = 6.5%), Tujia from Hunan (3/49 = 6.1%), Qiang (2/33 = 6.1%), Han Chinese (2/32 = 6.3% Han from Yili, Xinjiang, 4/66 = 6.1% Han from Huize, Yunnan, 2/35 = 5.7% Han from Meixian, Guangdong, 1/18 = 5.6% Han from Wuhan, Hubei, 6/148 = 4.1% Han from Changting, Fujian, 20/530 = 3.8% Han Chinese from Chongming Island,[32] 2/63 = 3.2% Han from Weicheng, Sichuan, 18/689 = 2.6% Han Chinese from Pudong,[32] 2/100 = 2.0% Han from Nanjing, Jiangsu, 3/165 = 1.8% Han Chinese, 1/55 = 1.8% Han from Shanghai), Manchus (1/50 = 2.0% Manchu from Liaoning[33]), and Koreans (2/133 = 1.5% Daejeon, 1/300 = 0.3% unrelated Korean males obtained from the National Biobank of Korea, 1/573 = 0.2% Seoul).

According to 23魔方, O-M7 has a TMRCA of approximately 14,530 years and is currently relatively common among many ethnic groups in Sichuan and Yunnan, as well as among the Zhuang, Austroasiatic, and Austronesian groups. O-M7 now accounts for about 2.15% of the total male population in China.[34] The O-N5 subclade (TMRCA 4,230 ybp) by itself accounts for about 0.40% of the total male population in China at present, with its proportion among Hmong-Mien-speaking populations in Southwest China being rather high; in regard to geography, it is found mainly in Guizhou (3.52% of the total provincial population), Hunan (1.63%), Chongqing (1.05%), Sichuan (0.83%), Guangxi (0.76%), Fujian (0.44%), Yunnan (0.35%), Guangdong (0.28%), Jiangxi (0.26%), Hubei (0.26%), Shaanxi (0.20%), and Ningxia (0.18%).[35]

O-M134

O-M134*

Paragroup O-M134(xM117) has been found with very high frequency in some samples of Kim Mun people, a subgroup of the Yao people of southern China (16/32 = 50.0% Mountain Kimmun from southern Yunnan, 11/28 = 39.3% Blue Kimmun from western Guangxi). However, this paragroup has been detected in only 3/41 = 7.3% of a sample of Lowland Kimmun from eastern Guangxi. This paragroup also has been found with high frequency in some Kazakh samples, especially the Naiman tribe (102/155 = 65.81%). Dulik hypothesizes that O-M134 in Kazakhs was due to a later expansion due to its much more recent TMRCA time.

The general outline of the distribution of O-M134(xM117) among modern populations is different as that of the related clade O-M117. In particular, O-M134(xM117) occurs with only low frequency or is nonexistent among most Tibeto-Burman-speaking populations of Southwest China, Northeast India, and Nepal, who exhibit extremely high frequencies of O-M117. This paragroup also occurs with very low frequency or is non-existent among most Mon-Khmer population of Laos, who exhibit much higher frequencies of O-M117. In Han Chinese, the paragroup is found in approximately the same percentage as O-M117, but has a higher distribution in northern Han Chinese than Southern Han Chinese.

According to 23魔方, the TMRCA of O-M134 is estimated to be 17,450 years, and O-M134(xM117) can be divided into two subsets: O-F122 (TMRCA 17,420 years), which is subsumed alongside O-M117 in an O-F450 clade (TMRCA 17,430 years), and O-MF59333 (TMRCA 13,900 years, currently distributed mainly in southern China and accounting for the Y-DNA of approximately 0.03% of the total male population of China), which is derived from O-M134 but basal to O-F450. O-F122 in turn is divided into O-MF38 (TMRCA 4,680 years, currently distributed mainly in northern China and accounting for the Y-DNA of approximately 0.02% of the total male population of China) and O-F114 (TMRCA 15,320 years, accounts for the Y-DNA of approximately 11.29% of the total male population of China). The O-F46 (TMRCA 10,050 years) subclade of O-F114 by itself accounts for the Y-DNA of approximately 10.07% of the total male population of present-day China.

In a study of Koreans from Seoul (n=573) and Daejeon (n=133), haplogroup O-M134(xM117), all members of which have been found to belong to O-F444 (phylogenetically equivalent to O-F114), has been found in 9.42% of the sample from Seoul and 10.53% of the sample from Daejeon.

In a study of Japanese (n=263), haplogroup O-M134(xM117) has been observed in nine individuals, or 3.4% of the entire sample set. The Japanese members of O-M134(xM117) in this study have originated from Shizuoka (3/12 = 25%), Tokyo (2/52 = 3.8%), Toyama (1/3), Ishikawa (1/4), Tochigi (1/5), and Ibaraki (1/5), respectively.[36]

O-M117

Haplogroup O2a2b1a1-M117 (also defined by the phylogenetically equivalent mutation Page23) is a subclade of O2a2b1-M134 that occurs frequently in China and in neighboring countries, especially among Tibeto-Burman-speaking peoples. Haplogroup O2a2b1a1-M117 is the most common Y-DNA haplogroup among present-day Chinese (16.27% China,[37] 59/361 = 16.3% Han Chinese, 397/2091 = 18.99% Han Chinese), followed closely by haplogroup O2a1b-IMS-JST002611.

O-M117 has been detected in samples of Tamang (38/45 = 84.4%)，Tibetans (45/156 = 28.8% or 13/35 = 37.1%), Tharus (57/171 = 33.3%), Han Taiwanese (40/183 = 21.9%), Newars (14/66 = 21.2%), the general population of Kathmandu, Nepal (13/77 = 16.9%), Han Chinese (5/34 = 14.7% Chengdu, 5/35 = 14.3% Harbin, 4/35 = 11.4% Meixian, 3/30 = 10.0% Lanzhou, 2/32 = 6.3% Yili), Tungusic peoples from the PRC (7/45 = 15.6% Hezhe, 4/26 = 15.4% Ewenki, 5/35 = 14.3% Manchu, 2/41 = 4.9% Xibe, 1/31 = 3.2% Oroqen), Koreans (4/25 = 16.0% Koreans from the PRC, 5/43 = 11.6% Koreans from South Korea), Mongols (5/45 = 11.1% Inner Mongolian, 3/39 = 7.7% Daur, 3/65 = 4.6% Outer Mongolian), and Uyghurs (2/39 = 5.1% Yili, 1/31 = 3.2% Urumqi).

Like O-M7, O-M117 has been found with greatly varying frequency in many samples of Hmong-Mien-speaking peoples, such as Mienic peoples (7/20 = 35.0% Mountain Straggler Mien, 9/28 = 32.1% Blue Kimmun, 6/19 = 31.6% Flower Head Mien, 3/11 = 27.3% Top Board Mien, 3/11 = 27.3% Thin Board Mien, 11/47 = 23.4% Western Mien, 6/33 = 18.2% Northern Mien, 5/31 = 16.1% Lowland Yao, 5/35 = 14.3% Yao from Liannan, Guangdong, 5/37 = 13.5% Zaomin, 5/41 = 12.2% Lowland Kimmun, 3/41 = 7.3% Native Mien, 2/31 = 6.5% Southern Mien, 2/32 = 6.3% Mountain Kimmun, but 0/35 Yao from Bama, Guangxi), She (6/34 = 17.6% She, 4/56 = 7.1% Northern She), and Hmongic peoples (9/100 = 9.0% Miao from Hunan, 4/51 = 7.8% Hmong Daw from northern Laos, 3/49 = 6.1% Miao from Yunnan, 1/49 = 2.0% Miao from Guizhou, but 0/36 Bunu from Guangxi).

In a study published by Chinese researchers in the year 2006, O-M117 has been found with high frequency (8/47 = 17.0%) in a sample of Japanese that should be from Kagawa Prefecture according to the geographical coordinates (134.0°E, 34.2°N) that have been provided. However, in a study published by Japanese researchers in the year 2007, the same haplogroup has been found with much lower frequency (11/263 = 4.2%) in a larger sample of Japanese from various regions of Japan. More precisely, the Japanese members of O-M117 in this study's sample set have originated from Tokyo (4/52), Chiba (2/44), Gifu (1/2), Yamanashi (1/2), Hiroshima (1/3), Aichi (1/6), and Shizuoka (1/12).

In Meghalaya, a predominantly tribal state of Northeast India, O-M133 has been found in 19.7% (14/71) of a sample of the Tibeto-Burman-speaking Garos, but in only 6.2% (22/353, ranging from 0/32 Bhoi to 6/44 = 13.6% Pnar) of a pool of eight samples of the neighboring Khasian-speaking tribes.

O-M333

PopulationFrequencynSourceSNPs
Derung1 
Naga
(Sagaing, Myanmar)		1.00015Page23=15
Nishi0.94 
Adi0.89 
Tamang0.86745M134
Nu0.86 
Yao (Liannan)0.82935M7=18
M117=5
M122(xM159, M7, M134)=4
M134(xM117)=2
Achang0.825 
Apatani0.82 
Bai0.82 
CHS
(Han in Hunan & Fujian)		0.78852M122=41
Naga (NE India)0.76534M134=26
Ava (Yunnan)0.75929M122
Han Chinese0.74 
She0.73534M7=10
M122(xM159, M7, M134)=7
M117=6
M134(xM117)=2
Nu0.7 
Miao0.7 
Shui0.7 
Han (Harbin)0.65735M122(xM159, M7, M134)=10
M134(xM117)=8
M117=5
Lisu0.65 
Zaomin (Guangdong)0.64937M122
She0.63 
Filipinos0.62 
Taiwan Han0.61921M122
Philippines0.60728M122
Han (East China)0.593167M122
Garo0.59 
Kinh (Hanoi, Vietnam)0.5848M122=28
Chin
(Chin State, Myanmar)		0.57919Page23=10
M122(xM324)=1
Han (North China)0.566129M122
Toba (Sumatra)0.55338P201(xM7, M134)
Northern Han0.55149M122
Garo0.55 
Tujia0.54 
Tujia0.53 
Han (Chengdu)0.52934M122(xM159, M7, M134)=8
M134(xM117)=5
M117=5
Han (NE China)0.52442M122=22
Han (Meixian)0.51435M122(xM159, M7, M134)=10
M117=4
M7=2
M159=1
M134(xM117)=1
CHB
(Han Chinese in Beijing)		0.50046F444=8
M117=7
JST002611=5
KL2(xJST002611)=2
M188(xM7)=1
Han (South China)0.49265M122
Va0.48 
Bai0.48
 
KHV
(Kinh in Ho Chi Minh City)		0.47846M7=6
M133=4
F444=4
JST002611=4
KL2(xJST002611)=2
N6>F4124=1
CTS1754=1
Koreans0.472216 
Lisu0.47 
Hani0.47 
Han (Yili)0.46932M122(xM159, M7, M134)=10
M7=2
M117=2
M134(xM117)=1
Bai (Dali, Yunnan)0.4650M122
Mongols (Baotou)0.45533F273=2
F4249=2
FGC23868=1
Z26109=1
F133=1
F12=1
Y26383=1
CTS201=1
F8=1
Y20928=1
F748=1
SK1783=1
SK1775=1
Hezhe (China)0.44445M122(xM159, M7, M134)=11
M134(xM117)=2
M117=7
Koreans0.443506P201=146
M324(xP201)=76
M122(xM324)=2
Tibetans
(Zhongdian, Yunnan)		0.44050M122
Miao0.44 
Yi0.44 
Lahu0.43 
Bit (Laos)0.42928M122
Manchu (NE China)0.426101M122=43
Koreans (Seoul)0.422573M122
Koreans (Daejeon)0.414133M122
Hmong Daw (Laos)0.41251M122
Vietnamese0.41 
Dai0.4 
Dungan (Kyrgyzstan)0.4040M122
Tibetans0.40035M117=13
M134(xM117)=1
Koreans (China)0.40025M122(xM159, M7, M134)=6
M117=4
Shan
(Northern Thailand)		0.40020M117=7
M7=1
Thai (Central Thailand)0.395129F8/F42*=17
M7=11
JST002611=10
F474/F317=4
F323/F46=4
M159=2
F2055/CTS445=1
F2137=1
F837=1
Koreans (South Korea)0.39543M122(xM159, M7, M134)=7
M134(xM117)=5
M117=5
Vietnamese0.39 
Khon Mueang
(Northern Thailand)		0.390205O-M117=46
O-M7=17
O-M324(xM7, M134)=16
O-M122(xM324)=1
Mon
(Northern Thailand)		0.38918M117=4
M324(xM7, M134)=3
Blang (Yunnan)0.38552M122
Northern Thai people
(Khon Mueang & Tai Yuan)		0.38486F8/F42=24
M7=7
JST002611=1
F999/F717=1
Manchu0.38 
Philippine
(Tagalog language group)		0.38050M122
Hanoi, Vietnam0.37524M7=3
M134(xM133)=3
M133=1
JST002611=1
M159=1
Manchu0.37135M122(xM159, M7, M134)=6
M117=5
M134(xM117)=2
Han (Lanzhou)0.36730M122(xM159, M7, M134)=6
M117=3
M134(xM117)=2
Lahu0.36 
Qiang0.36433M134(xM117)=4
M117=3
M122(xM159, M7, M134)=3
M7=2
Bamar (Myanmar)0.36172Page23=26
Borneo, Indonesia0.36086M122
Korean0.35645M122
Pahng (Guangxi)0.35531M122
Philippines0.35448M122
Western Yugur0.35 
Thai
(Chiang Mai & Khon Kaen)		0.35334
M122
Tai Yong
(Northern Thailand)		0.34626M324(xM7, M134)=4
M117=3
M7=2
Tharu0.345171M134
Kinh (Hanoi, Vietnam)0.34276M122
Koreans (Seoul)0.34185M122=29
Tibet0.340156M122
Yao (Bama)0.34335M7=12
Kazakhs (SE Altai)0.33789M134(xM117, P101)
Tai Yuan
(Thailand)		0.32985M117=15
M7=5
M122(xM324)=5
M134(xM117)=3
Dai
(Xishuangbanna, Yunnan)		0.32752O-M133=13
O-M7=2
O-F444=1
O-JST002611=1
Polynesians0.325 
Tibetans0.32 
Khasi0.32 
Lao
(Luang Prabang, Laos)		0.3225M122
Eastern Yugur0.31 
Malays0.31 
Buyei0.31435M7=6
M134(xM117)=3
M117=1
M122(xM159, M7, M134)=1
Mongolian (Khalkh)0.311 
Filipinos0.308146P164(xM134)=26
JST002611=7
M7=3
M133=3
M134(xM133)=2
P201(xM159, M7, P164)=2
M159=1
M324(xKL1, P201)=1
Han (Pinghua speakers)0.3 
Salar0.30243M122
Dong0.30020M134=3
M122(xM7, M134)=3
Thailand0.29375M133(xM162)=10
M7=5
M134(xM133)=3
JST002611=2
P164(xM134)=1
M122(xM324)=1
Koreans (NE China)0.29179M122=23
Khasi0.29 
Zhuang0.29 
Inner Mongolian0.28945M122(xM159, M7, M134)=5
M117=5
M134(xM117)=3
Tai Lue
(Northern Thailand)		0.28691O-M117=16
O-M7=6
O-M324(xM7, M134)=3
O-M122(xM324)=1
Zhuang0.28628M134=7
M122(xM7, M134)=1
Laotian
(Vientiane & Luang Prabang)		0.27540F8/F42=6
M7=2
M188(xM7)=2
P164(xF8,F46,F4110,F706,F717)=1
Bonan0.27344M122
Sibe0.26841M134(xM117)=5
M122(xM159, M7, M134)=4
M117=2
Micronesia0.27 
Mon (Thailand)0.267105F8/F42=15
M7=4
F323/F46=4
JST002611=3
F2859=1
M122(x002611,M188,P164,F837)=1
Daur0.25639M122(xM159, M7, M134)=7
M117=3
Polynesians0.25
 
Bunu (Guangxi)0.2536M122
Malay
(near Kuala Lumpur)		0.2512M122
Zhuang (Guangxi)0.247166M122(xM121, M134)=23
M117=9
M134(xM117)=7
M121=2
Japanese (Kyūshū)0.240104M122
Dongxiang0.24 
Manchurian Evenks0.24 
Thai (Northern Thailand)0.23517M122
Japanese (Kagawa)0.23447M117=8
M134(xM117)=2
M122(xM159, M7, M134)=1
Mosuo (Ninglang, Yunnan)0.23447M122
Evenks (China)0.23126M117=4
M134(xM117)=1
M122(xM159, M7, M134)=1
Mongolia
(mainly Khalkhs) 		0.228149M134=24
M122(xM134)=10
Zhuang
(Napo County, Guangxi)		0.22263M117=5
M122(xM188, M134)=4
M188=3
M134(xM117)=2
Lawa
(Northern Thailand)		0.22050M324(xM7, M134)=6
M117=5
Mal (Laos)0.22050M122
Cambodian (Siem Reap)0.216125M122
Japanese (Tokushima)0.21470M134=11
M122(xM134, LINE)=2
LINE=2
Newar0.21266M117
Lao Isan0.21062M7=6
F8=4
JST002611=3
Blang0.21 
Okinawans0.21 
Tai Khün
(Northern Thailand)		0.20824M117=4
M134(xM117)=1
Kathmandu, Nepal0.20877M324
Sui0.20050M134=10
Yi (Shuangbai, Yunnan)0.2050M122(xM7)
Japanese (Shizuoka)0.19761M122(xM134, LINE)=7
M134=5
Khmu (Laos)0.19651M122
Dongxiang0.19646M122
Oroqen0.19431M122(xM159, M7, M134)=2
M7=2
M134(xM117)=1
M117=1
Khalkh (Mongolia)0.18885M122=16
Japanese (Miyazaki)0.1831285M134=118
M122(xM134)=117
Japanese (Tokyo)0.17956M117=5
M134(xM117)=3
JST002611=2
Hani0.17634M134(xM117)=3
M117=2
M122(xM159, M7, M134)=1
Micronesia0.17617M122(xM134, LINE)=3
Hui0.17135M122(xM159, M7, M134)=4
M134(xM117)=1
M117=1
Kalmyk (Khoshuud)0.17182M122=14
Japanese0.167263M122
Mandar (Sulawesi)0.16754M122
Mulam (Luocheng)0.16742JST002611=3
M134(xM117)=3
M117=1
Japanese (Kantō)0.162117M122=19
Thai0.16 
Zhuang0.16 
Aheu (Laos)0.15838M122
Bugan (Yunnan)0.15632M122
Okinawans0.15645M122(xM134, LINE)=3
LINE=3
M134=1
Uygur (Yili)0.15439M122(xM159, M7, M134)=2
M134(xM117)=2
M117=2
Japanese (Aomori)0.15426M134=3
M122(xM134, LINE)=1
Cambodia0.14 
Cham
(Binh Thuan, Vietnam)		0.13659M122
Java
(mainly sampled in Dieng)		0.13161M122
Aboriginal Taiwanese0.126223M122
Uighur (Kazakhstan)0.12241M122
Uzbek (Bukhara)0.12158M122
Ulchi0.11552O-M122(xP201)=6
Karakalpak (Uzbekistan)0.11444M122
Utsat (Sanya, Hainan)0.11172M117=3
M122(xM159, M117)=3
M159=2
Outer Mongolian0.10865M122(xM159, M7, M134)=3
M117=3
M134(xM117)=1
Bo (Laos)0.10728M122
Tibetans0.1 
Maluku Islands0.130M122
Kazakh (Kazakhstan)0.09354M122
Bouyei0.08945M122(xM7, M134)=2
M7=1
M134=1
Pumi (Ninglang, Yunnan)0.08547M122(xM7)
Zakhchin (Mongolia)0.08360M122=5
Mongols0.08324M122
Balinese (Bali)0.073641M122
Japanese0.06859P198
Uriankhai (Mongolia)0.06760M122=4
Sinte (Uzbekistan)0.06715M122
Uygur (Urumqi)0.06531M134(xM117)=1
M117=1
Iranian (Esfahan)0.06316M122
Kalmyk (Dörwöd)0.061165M122=10
Flores0.046394M122
Buryat0.040298M324(xM134)=5
M134(xM117)=4
M117=3
Buyei0.04 
Kalmyk (Torguud)0.033150M122=5
Kazakhs (SW Altai)0.03330M134(xM117, P101)
Munda (Jharkhand)0.03294M134=3
Burusho0.03197M122
Li0.02934M134(xM117)=1
Sumba0.029350M122
Khoton (Mongolia)0.02540M122=1
Naxi (Lijiang, Yunnan)0.02540M134
Rajbanshi
(West Bengal)		0.02245M134=1
Pathan0.01096M122
Pakistan0.005638M122

Phylogenetics

Phylogenetic History

See main article: Conversion table for Y chromosome haplogroups. Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008 (Shorthand)(α)(β)(γ)(δ)(ε)(ζ)(η)YCC 2002 (Longhand)YCC 2005 (Longhand)YCC 2008 (Longhand)YCC 2010r (Longhand)ISOGG 2006ISOGG 2007ISOGG 2008ISOGG 2009ISOGG 2010ISOGG 2011ISOGG 2012
O-M17526VII1U28Eu16H9IO*OOOOOOOOOO
O-M11926VII1U32Eu16H9HO1*O1aO1aO1aO1aO1aO1aO1aO1aO1aO1a
O-M10126VII1U32Eu16H9HO1aO1a1O1a1aO1a1aO1a1O1a1O1a1aO1a1aO1a1aO1a1aO1a1a
O-M5026VII1U32Eu16H10HO1bO1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2
O-P3126VII1U33Eu16H5IO2*O2O2O2O2O2O2O2O2O2O2
O-M9526VII1U34Eu16H11GO2a*O2aO2aO2aO2aO2aO2aO2aO2aO2a1O2a1
O-M8826VII1U34Eu16H12GO2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1aO2a1a
O-SRY46520VII1U35Eu16H5IO2b*O2bO2bO2bO2bO2bO2bO2bO2bO2bO2b
O-47z5VII1U26Eu16H5IO2b1O2b1aO2b1O2b1O2b1aO2b1aO2b1O2b1O2b1O2b1O2b1
O-M12226VII1U29Eu16H6LO3*O3O3O3O3O3O3O3O3O3O3
O-M12126VII1U29Eu16H6LO3aO3aO3a1O3a1O3a1O3a1O3a1O3a1O3a1O3a1aO3a1a
O-M16426VII1U29Eu16H6LO3bO3bO3a2O3a2O3a2O3a2O3a2O3a2O3a2O3a1bO3a1b
O-M15913VII1U31Eu16H6LO3cO3cO3a3aO3a3aO3a3O3a3O3a3aO3a3aO3a3aO3a3aO3a3a
O-M726VII1U29Eu16H7LO3d*O3cO3a3bO3a3bO3a4O3a4O3a3bO3a3bO3a3bO3a2bO3a2b
O-M11326VII1U29Eu16H7LO3d1O3c1O3a3b1O3a3b1-O3a4aO3a3b1O3a3b1O3a3b1O3a2b1O3a2b1
O-M13426VII1U30Eu16H8LO3e*O3dO3a3cO3a3cO3a5O3a5O3a3cO3a3cO3a3cO3a2c1O3a2c1
O-M11726VII1U30Eu16H8LO3e1*O3d1O3a3c1O3a3c1O3a5aO3a5aO3a3c1O3a3c1O3a3c1O3a2c1aO3a2c1a
O-M16226VII1U30Eu16H8LO3e1aO3d1aO3a3c1aO3a3c1aO3a5a1O3a5a1O3a3c1aO3a3c1aO3a3c1aO3a2c1a1O3a2c1a1

Original Research Publications

The following research teams per their publications were represented in the creation of the YCC Tree.

Phylogenetic Trees

This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree. and subsequent published research.

See also

Y-DNA Backbone Tree

References

Sources

Journal articles
Websites

External links

Notes and References

  1. Karmin . Monika . Flores . Rodrigo . Saag . Lauri . Hudjashov . Georgi . Brucato . Nicolas . Crenna-Darusallam . Chelzie . Larena . Maximilian . Endicott . Phillip L. . Jakobsson . Mattias . Lansing . J. Stephen . Sudoyo . Herawati . Leavesley . Matthew . Metspalu . Mait . Ricaut . François-Xavier . Cox . Murray P. . 4 . Episodes of Diversification and Isolation in Island Southeast Asian and Near Oceanian Male Lineages . Molecular Biology and Evolution . 28 February 2022 . 39 . 3 . 0737-4038 . 10.1093/molbev/msac045 . 35294555 . 8926390.
  2. Web site: Krahn . Thomas . FTDNA . 2003 . Genomic Research Center Draft Tree (AKA Y-TRee) . https://web.archive.org/web/20150815071342/http://ytree.ftdna.com/index.php?name=Draft . 2015-08-15.
  3. Bing Su . Chunjie Xiao . Ranjan Deka . Mark T. Seielstad . Daoroong Kangwanpong . Junhua Xiao . Daru Lu . Peter Underhill . Luca Cavalli-Sforza . Ranajit Chakraborty . Li Jin . 4 . Y chromosome haplotypes reveal prehistorical migrations to the Himalayas . Human Genetics . 2000 . 107 . 582-590 . 10.1007/s004390000406 .
  4. Jatupol Kampuansai, Wibhu Kutanan, Eszter Dudás, Andrea Vágó-Zalán, Anikó Galambos, and Horolma Pamjav (2020), "Paternal genetic history of the Yong population in northern Thailand revealed by Y-chromosomal haplotypes and haplogroups." Molecular Genetics and Genomics volume 295, pages 579–589. https://doi.org/10.1007/s00438-019-01644-x
  5. Karmin . Monika . Saag . Lauri . Vicente . Mário . Wilson Sayres . Melissa A. . etal . 2015 . A recent bottleneck of Y chromosome diversity coincides with a global change in culture . Genome Research . 25 . 4. 459–466 . 10.1101/gr.186684.114 . 25770088 . 4381518.
  6. Web site: 23魔方 [23 Rubik's Cube] . O-M122单倍群详情 . zh.
  7. Yong-Bin . Zhao . Ye . Zhang . Quan-Chao . Zhang . Hong-Jie . Li . Ying-Qiu . Cui . Zhi . Xu . Li . Jin . Hui . Zhou . Hong . Zhu . 4 . May 4, 2015 . Ancient DNA Reveals That the Genetic Structure of the Northern Han Chinese Was Shaped Prior to 3,000 Years Ago . PLOS ONE . 10 . 5 . e0125676 . 10.1371/journal.pone.0125676 . 25938511 . 4418768 . 2015PLoSO..1025676Z . free.
  8. Shi . Yan . Chuan-Chao . Wang . Hong-Xiang . Zheng . Wei . Wang . Zhen-Dong . Qin . Lan-Hai . Wei . Yi . Wang . Xue-Dong . Pan . Wen-Qing . Fu . Yun-Gang . He . Li-Jun . Xiong . Wen-Fei . Jin . Shi-Lin . Li . Yu . An . Hui . Li . Li . Jin . 4 . August 29, 2014 . Y Chromosomes of 40% Chinese Descend from Three Neolithic Super-Grandfathers . PLOS ONE . 9 . 8 . e105691 . 10.1371/journal.pone.0105691 . 25170956 . 4149484 . 1310.3897 . 2014PLoSO...9j5691Y . free.
  9. 10.1038/srep38656. 27924949. 5141421. Genetic evidence for an East Asian origin of Chinese Muslim populations Dongxiang and Hui. Scientific Reports. 6. 38656. 2016. Yao. Hong-Bing. Wang. Chuan-Chao. Tao. Xiaolan. Shang. Lei. Wen. Shao-Qing. Zhu. Bofeng. Kang. Longli. Jin. Li. Li. Hui. 2016NatSR...638656Y. 4.
  10. PhD . Murray P. . Cox . Genetic Patterning at Austronesian Contact Zones . June 2003 . University of Otago . 15 January 2022 . 5 September 2006 . https://web.archive.org/web/20060905193504/http://www.u.arizona.edu/~mpcox/publications/Cox_2003_PhD.pdf.
  11. Shi . Hong . Dong . Yong-li . Wen . Bo . Xiao . Chun-Jie . Underhill . Peter A. . Shen . Pei-dong . Chakraborty . Ranajit . Jin . Li . Su . Bing . 4 . Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O2-M122 . 1226206 . American Journal of Human Genetics . 77 . 408–419. 408–19 . 10.1086/444436 . 16080116 . Sep 2005.
  12. Peng . Min-Sheng . He . Jun-Dong . Fan . Long . Liu . Jie . Adeola . Adeniyi C. . Wu . Shi-Fang . Murphy . Robert W. . Yao . Yong-Gang . Zhang . Ya-Ping . 4 . August 2014 . Retrieving Y chromosomal haplogroup trees using GWAS data . European Journal of Human Genetics . 22 . 8. 1–5 . 10.1038/ejhg.2013.272 . free . 4350590 . 24281365. Published online 27 November 2013.
  13. https://isogg.org/tree/ISOGG_HapgrpO.html ISOGG Y-DNA Haplogroup O and its Subclades - 2017
  14. Web site: 23魔方 [23 Rubik's Cube] . Phylogenetic tree of human Y-DNA . zh.
  15. https://www.yfull.com/tree/O/ YFull
  16. Wang . Chuan-Chao . Wang . Ling-Xiang . Shrestha . Rukesh . Zhang . Manfei . Huang . Xiu-Yuan . Hu . Kang . Jin . Li . Li . Hui . 2014 . Genetic Structure of Qiangic Populations Residing in the Western Sichuan Corridor . PLOS ONE . 9 . 8. e103772 . 10.1371/journal.pone.0103772 . 25090432 . 4121179. 2014PLoSO...9j3772W . free.
  17. Wang . Chuan-Chao . Yan . Shi . Qin . Zhen-Dong . Lu . Yan . Ding . Qi-Liang . Wei . Lan-Hai . Li . Lin-Shi . Yang . Ya-Jun . Jin . Li . Li . Hui . 4 . 2013 . Late Neolithic expansion of ancient Chinese revealed by Y chromosome haplogroup O2a1c-JST002611 . Journal of Systematics and Evolution . 51 . 3. 280–286 . 10.1111/j.1759-6831.2012.00244.x. 55081530 . free.
  18. Kwon . So Yeun . Lee . Hwan Young . Lee . Eun Young . Yang . Woo Ick . Shin . Kyoung-Jin . 2015 . Confirmation of Y haplogroup tree topologies with newly suggested Y-SNPs for the C2, O2b and O3a subhaplogroups . Forensic Science International: Genetics . 19 . 42–46 . 10.1016/j.fsigen.2015.06.003 . 26103100.
  19. Web site: O-Ims-Jst002611单倍群详情 . 23魔方 [23 Rubik's Cube] . zh.
  20. Guanglin He . Mengge Wang . Lei Miao . Jing Chen . Jie Zhao . Qiuxia Sun . Shuhan Duan . Zhiyong Wang . Xiaofei Xu . Yuntao Sun . Yan Liu . Jing Liu . Zheng Wang . Lanhai Wei . Chao Liu . Jian Ye . Le Wang . 4 . Multiple founding paternal lineages inferred from the newly-developed 639-plex Y-SNP panel suggested the complex admixture and migration history of Chinese people . Human Genomics . 17 . 29 . 2023 . 10.1186/s40246-023-00476-6 . free. 10045532 .
  21. Web site: 23魔方 [23 Rubik's Cube] . O-M188单倍群详情 . zh.
  22. Web site: 23魔方 [23 Rubik's Cube] . O-Am01822单倍群详情 . zh.
  23. Web site: 23魔方 [23 Rubik's Cube] . zh . O-M134单倍群详情.
  24. Web site: O-M7单倍群详情 . 23魔方 [23 Rubik's Cube] . zh .
  25. Web site: 23魔方 [23 Rubik's Cube] . zh . O-Cts201单倍群详情.
  26. Web site: 23魔方 [23 Rubik's Cube] . zh . O-Mf109044单倍群详情.
  27. Web site: 23魔方 [23 Rubik's Cube] . O-M134单倍群详情 . zh.
  28. Web site: 23魔方 [23 Rubik's Cube] . O-Am01822单倍群详情 . zh.
  29. Web site: 23魔方 [23 Rubik's Cube] . O-M159单倍群详情 . zh.
  30. Enrico Macholdt, Leonardo Arias, Nguyen Thuy Duong, et al., "The paternal and maternal genetic history of Vietnamese populations." European Journal of Human Genetics (2020) 28:636–645. https://doi.org/10.1038/s41431-019-0557-4
  31. Frederick Delfin . Jazelyn M Salvador . Gayvelline C Calacal . Henry B Perdigon . Kristina A Tabbada . Lilian P Villamor . Saturnina C Halos . Ellen Gunnarsdóttir . Sean Myles . David A Hughes . Shuhua Xu . Li Jin . Oscar Lao . Manfred Kayser . Matthew E Hurles . Mark Stoneking . Maria Corazon A De Ungria . 4 . The Y-chromosome landscape of the Philippines: extensive heterogeneity and varying genetic affinities of Negrito and non-Negrito groups . European Journal of Human Genetics . February 2011 . 19 . 224–230 . 10.1038/ejhg.2010.162 . free. 3025791 . Published online 29 September 2010.
  32. Zhang X, Tang Z, Wang B, Zhou X, Zhou L, Zhang G, Tian J, Zhao Y, Yao Z, Tian L, Zhang S, Xia H, Jin L, Li C, Li S . 4 . Forensic Analysis and Genetic Structure Construction of Chinese Chongming Island Han Based on Y Chromosome STRs and SNPs . Genes . 2022 . 13 . 8 . 1363 . 10.3390/genes13081363 . free. 9407086 .
  33. Karafet TM, Osipova LP, Savina OV, Hallmark B, Hammer MF . Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations . American Journal of Human Biology . November–December 2018 . 30 . 6 . e23194 . 10.1002/ajhb.23194.
  34. Web site: O-M7单倍群详情 . 23魔方 [23 Rubik's Cube] . zh.
  35. Web site: 夏商西南大族祖源分析-23魔方祖源基因检测 . 23魔方 [23 Rubik's Cube] . zh.
  36. Sae Naitoh . Iku Kasahara-Nonaka . Kiyoshi Minaguchi . Phrabhakaran Nambiar . Assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree . Journal of Human Genetics . 2013 . 58 . 195–201 . 10.1038/jhg.2012.159 . free.
  37. Web site: 23魔方 [23 Rubik's Cube] . zh . O-M117单倍群详情.

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Haplogroup O-M122".

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