The Genome Variation Map (GVM) is a public data repository of genome variations, including single nucleotide polymorphisms and small insertions and deletions, with particular focuses on human as well as cultivated plants and domesticated animals.
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All species with genomic variants
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How to Cite

When you have successfully submitted data to GVM, please consider to use the following words to describe data deposition in your manuscript.

The variation data reported in this paper has been deposited in the Genome Variation Map [1] in National Genomics Data Center [2], China National Center for Bioinformation / Beijing Institute of Genomics, Chinese Academy of Sciences, under accession number GVMXXXXXX that can be publicly accessible at http://bigd.big.ac.cn/gvm/getProjectDetail?project=GVMXXXXXX

1. Genome Variation Map: a worldwide collection of genome variations across multiple species. Nucleic Acids Res 2021, 49(D1):D1186-D1191.[PMID=33170268].
2. Database Resources of the National Genomics Data Center, China National Center for Bioinformation in 2024. Nucleic Acids Res 2024, 52(D1):D18-D32. [PMID=38018256].
3. GWAS Atlas: an updated knowledgebase integrating more curated associations in plants and animals. Nucleic Acids Res 2023, 51(D1):D969–D976.[PMID=36263826].

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Email: gvm@big.ac.cn

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Variants related resources

GWAS Atlas
European Variation Archive(EVA)
● NCBI-based platforms:
ClinVar
dbGaP
dbSNP
dbVar

Newsmore>>

  A total of 103,916,633 SNPs derived from 414 Triticum aestivum (Bread Wheat) accessions are integrated into GVM.(2022-09-19)