A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696714



Internal ID15086680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61920582..62021174hg38UCSC Ensembl
Innerchr15:62212781..62313373hg19UCSC Ensembl
Innerchr15:60000073..60100665hg18UCSC Ensembl
Innerchr15:60000073..60100665hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38100593
hg19100593
hg18100593
hg17100593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516639
Supporting Variants
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696714
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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