A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704583



Internal ID15094549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60149439..60163403hg38UCSC Ensembl
Innerchr17:58226800..58240764hg19UCSC Ensembl
Innerchr17:55581582..55595546hg18UCSC Ensembl
Innerchr17:55581582..55595546hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3813965
hg1913965
hg1813965
hg1713965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528050
Supporting Variants
Samples
Known GenesCA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704583
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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