A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694505



Internal ID15431157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35927776..35927834hg38UCSC Ensembl
Innerchr15:36219977..36220035hg19UCSC Ensembl
Innerchr15:34007269..34007327hg18UCSC Ensembl
Innerchr15:34007269..34007327hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
hg1759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521741
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694505
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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