A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518659



Internal ID15099266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73223574..73234975hg38UCSC Ensembl
Innerchr11:72934619..72946020hg19UCSC Ensembl
Innerchr11:72612267..72623668hg18UCSC Ensembl
Innerchr11:72612267..72623668hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3811402
hg1911402
hg1811402
hg1711402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696109
Samples
Known GenesP2RY2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518659
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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