A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694908



Internal ID15431560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38970771..39156486hg38UCSC Ensembl
Innerchr15:39262972..39448687hg19UCSC Ensembl
Innerchr15:37050264..37235979hg18UCSC Ensembl
Innerchr15:37050264..37235979hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38185716
hg19185716
hg18185716
hg17185716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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