ID: | NBDC01392 |
Database name: | HGVD |
Alternative name: | Human Genetic Variation Database |
URL: | http://www.genome.med.kyoto-u.ac.jp/SnpDB/index.html |
Database maintenance site: | Kyoto University (Link to J-Global) |
Country/Region: | Japan |
Database description: | 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. |
Organism(s) covered: | Homo sapiens (9606) |
Tag - Target: | Genome/Gene, Genetic variation, Health/Disease |
Tag - Information type: | Sequence |
Reference(s) - PubMed ID/DOI: | - |
Language(s): | English |
Operational status: | Active |
Link(s) to Downloadable data: | http://www.genome.med.kyoto-u.ac.jp/SnpDB/download.html |
Link(s) to Metadata of downloadable data: | - |
Link(s) to Terms of use: | http://www.genome.med.kyoto-u.ac.jp/SnpDB/about.html |
Link(s) to "How to use": | - |
Contact information of database: | - |
Link(s) to API / SPARQL endpoint | - |