Population Genomics and Genetics-SNV

人类单核苷酸变异群体基因组学与遗传学数据库，收录了268,890,619个SNVs变异位点，涵盖220,147个基因组样本和1,018个古代基因组，涉及977个族群，用于理解人类单核苷酸变异在不同群体中的进化与医学意义。The Human Population Genomic and Genetic Database of Single Nucleotide Variants (SNVs) houses 268,890,619 SNV loci, covering 220,147 modern genomic samples and 1,018 ancient genomes, and spanning 977 ethnic groups. It is designed to facilitate the understanding of the evolutionary and medical significance of human single nucleotide variants across diverse populations.

搜集汇总

背景与挑战

背景概述

该数据库专注于人类单核苷酸变异的群体基因组学和遗传学研究，收录了超过2.68亿个SNV变异位点，涵盖约22万个现代基因组样本和千余个古代基因组，涉及近千个族群，旨在解析这些变异在群体中的进化与医学意义。