Haplogroup Q-P89.1 is a subclade of Y-DNA Haplogroup Q-MEH2.[1] Haplogroup Q-P89.1 is defined by the presence of the P89.1
Single Nucleotide Polymorphism (SNP). In 2010, Q-P89.1 was reclassified as "private" and removed from the haplotree.[2]
Distribution
Q-P89.1 has descendants in the
Northwest Territory of modern
Canada. It was in pre-Columbian American populations that it was discovered.[1][3]
The Americas
Q-P89.1 is present in
pre-Columbian populations in the Canadian Northwest.[1]
^Van Oven M, Van Geystelen A, Kayser M, Decorte R, Larmuseau HD (2014). "Seeing the wood for the trees: a minimal reference phylogeny for the human Y chromosome". Human Mutation. 35 (2): 187–91.
doi:
10.1002/humu.22468.
PMID24166809.
S2CID23291764.
^K-M2313*, which as yet has no phylogenetic name, has been documented in two living individuals, who have ethnic ties to India and South East Asia. In addition, K-Y28299, which appears to be a primary branch of K-M2313, has been found in three living individuals from India. See: Poznik op. cit.;
YFull YTree v5.08, 2017, "K-M2335", and;
PhyloTree, 2017, "Details of the Y-SNP markers included in the minimal Y tree" (Access date of these pages: 9 December 2017)
^ Haplogroup S, as of 2017, is also known as K2b1a. (Previously the name Haplogroup S was assigned to K2b1a4.)
^ Haplogroup M, as of 2017, is also known as K2b1b. (Previously the name Haplogroup M was assigned to K2b1d.)