A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694494



Internal ID15431146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21801783..21809114hg38UCSC Ensembl
Innerchr13:22375922..22383253hg19UCSC Ensembl
Innerchr13:21273922..21281253hg18UCSC Ensembl
Innerchr13:21273922..21281253hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg387332
hg197332
hg187332
hg177332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521733
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694494
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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