A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698876



Internal ID15435528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19868094..20021049hg38UCSC Ensembl
Innerchr9:19868092..20021047hg19UCSC Ensembl
Innerchr9:19858092..20011047hg18UCSC Ensembl
Innerchr9:19858092..20011047hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38152956
hg19152956
hg18152956
hg17152956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523164
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698876
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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