A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661491



Internal ID15398143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24109283..24226855hg38UCSC Ensembl
Innerchr15:24354430..24472002hg19UCSC Ensembl
Innerchr15:21905523..22023095hg18UCSC Ensembl
Innerchr15:21905523..22023095hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38117573
hg19117573
hg18117573
hg17117573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known GenesPWRN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661491
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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