A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569277



Internal ID16356686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43845555..43855067hg38UCSC Ensembl
Innerchr15:44137753..44147265hg19UCSC Ensembl
Innerchr15:41925045..41934557hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg389513
hg199513
hg189513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842396
Samples
Known GenesWDR76
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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