Rsrc
J-GLOBAL ID:201410045562678570   Research Resource code:NBDC00037 Update date:Jun. 04, 2015

Database of Genomic Variants: A curated catalogue of structural variation in the human genome

Database of Genomic Variants: A curated catalogue of structural variation in the human genome
Owning Organization:
  • The Centre for Applied Genomics
Resource classification: Database
Tag (subject)  (2): Genetic variation ,  Health/Disease
Tag (data type)  (1): Sequence
Species (1): Homo sapiens (NCBI Taxonomy ID: 9606)
Overview:
Database of Genomic Variants is a repository that provides information about variations in structure in the human genome.

The database offers information on genomic changes in DNA segments larger than 1kb as well as annotated insertion/deletion variations in a range of 100bp to 1kb. Only healthy samples were studied, which makes the results very useful to apply as controls in future related studies.

The collection contains 101,923 entries.

The number of CNVs identified is 6,6741 and inversions are 953.

There were 34,229 InDels in the 100bp to 1kb range.

Data concerning whole chromosomes can be retrieved.

Keyword and Blast search options are also provided.
Source: NBDC
Record maintainer: Integbio Database Catalog
Record license: Creative Commons CC0 license

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