A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861693



Internal ID15808963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79169293..79234387hg38UCSC Ensembl
Innerchr16:79203190..79268284hg19UCSC Ensembl
Innerchr16:77760691..77825785hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3865095
hg1965095
hg1865095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573287
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)nssv861693
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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