A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521762



Internal ID15102369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68057555..68179553hg38UCSC Ensembl
Innerchr15:68349893..68471891hg19UCSC Ensembl
Innerchr15:66136947..66258945hg18UCSC Ensembl
Innerchr15:66136947..66258945hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38121999
hg19121999
hg18121999
hg17121999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694530
Samples
Known GenesPIAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521762
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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