A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861606



Internal ID16155562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78471101..78783332hg38UCSC Ensembl
Innerchr16:78504998..78817229hg19UCSC Ensembl
Innerchr16:77062499..77374730hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38312232
hg19312232
hg18312232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573260
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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