A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615260



Internal ID16402669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116963446..117037305hg38UCSC Ensembl
Innerchr9:119725725..119799584hg19UCSC Ensembl
Innerchr9:118765546..118839405hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3873860
hg1973860
hg1873860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141287
Samples
Known GenesASTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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