Rsrc
J-GLOBAL ID：201710016047447258
Research Resource code：NBDC01653
Update date：Jun. 11, 2017
dbDNV: Duplicated-gene Nucleotide Variants
dbDNV: Duplicated-gene Nucleotide Variants
Owning Organization：
Resource classification：
Data,Database
Tag (subject) (3)：
Genome/Gene
, Genetic variation
, Organism
Tag (data type) (1)：
Sequence
Species (1)：
Homo sapiens (NCBI Taxonomy ID: 9606)
Overview：
The dbDNV is a database about duplicated gene nucleotide variants (DNVs), which assist users to distinguish DNVs from single nucleotide polymorphisms (SNPs). It allows users obtain duplicated gene loci (DGL) by querying via the NCBI accession number of a reference transcript. Users can also browse the identified DNVs in the genomic order by clicking the chromosome name, and also get a list of DNVs after specifying a chromosome or a genomic region. By using IDs of the existing SNP records in dbSNP, users can find the DNVs located on the same genomic position of the SNPs.
Source：
NBDC
Record maintainer：
Integbio Database Catalog
Record license：
Creative Commons CC0 license
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