A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691351



Internal ID15428003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24136736..24188295hg38UCSC Ensembl
Innerchr15:24381883..24433442hg19UCSC Ensembl
Innerchr15:21932976..21984535hg18UCSC Ensembl
Innerchr15:21932976..21984535hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3851560
hg1951560
hg1851560
hg1751560
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)nssv691351
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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