dbVar

E569114

dbVar is a public NCBI database that archives and provides access to human genomic structural variation data, such as insertions, deletions, and copy number variants.

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Statements (48)

Predicate Object
instanceOf NCBI database
genomic database
structural variation database
accessibleVia NCBI E-utilities API NERFINISHED
NCBI website NERFINISHED
web browser
accessPolicy open access without registration
aimsTo standardize representation of structural variants
support research on genomic structural variation
archives complex genomic rearrangements
copy number variants
copy number variation
deletions
duplications
insertions
inversions
countryOfOperator United States of America
surface form: United States
dataSource clinical and research submissions
large-scale genomic projects
published studies
dataType genomic structural variation data
human genomic variation data
sequence-level variation annotations
focusesOn human genomic structural variation
structural variants
hasIdentifierPrefix esv
nsv
ssv
hasPrimaryURL https://www.ncbi.nlm.nih.gov/dbvar
hostedOn NCBI infrastructure NERFINISHED
integratedWith ClinVar NERFINISHED
NCBI Gene NERFINISHED
NCBI Genome Data Viewer NERFINISHED
dbSNP NERFINISHED
license free public access
maintainedBy NCBI NERFINISHED
National Center for Biotechnology Information NERFINISHED
operatedBy National Center for Biotechnology Information NERFINISHED
partOf NCBI Entrez system NERFINISHED
primarySpecies Homo sapiens
provides downloadable variant datasets
links to related NCBI resources
public access to structural variation data
search interface for structural variants
subjectArea bioinformatics
genomics
human genetics
supportsSpecies Homo sapiens NERFINISHED

Referenced by (1)

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