Rsrc
J-GLOBAL ID：201410060986106885
Research Resource code：NBDC01392
Update date：May. 01, 2014
HGVD: Human Genetic Variation Database
HGVD: Human Genetic Variation Database
Resource classification：
Data,Database
Tag (subject) (3)：
Genome/Gene
, Genetic variation
, Health/Disease
Tag (data type) (1)：
Sequence
Species (1)：
Homo sapiens (NCBI Taxonomy ID: 9606)
Overview：
HGVD is a database providing a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. It contains genetic variations determined by exome sequencing of 1,208 individuals and genotyping data of common variations obtained from a cohort of 3,248 individuals. This database includes information such as alleles, genotype frequencies, number of samples, coverages, and expression QTL (eQTL) significances. The HGVD browser allows to search using gene name / ID, rsID of dbSNP, pathogenic variation, or chromosome numbers.
Source：
NBDC
Record maintainer：
Integbio Database Catalog
Record license：
Creative Commons CC0 license
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