A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688082



Internal ID15424734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24359755..24569435hg38UCSC Ensembl
Innerchr15:24604902..24814582hg19UCSC Ensembl
Innerchr15:22155995..22365675hg18UCSC Ensembl
Innerchr15:22155995..22365675hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38209681
hg19209681
hg18209681
hg17209681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known GenesPWRN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688082
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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