A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv860802



Internal ID16154758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78137789..78138277hg38UCSC Ensembl
Innerchr16:78171686..78172174hg19UCSC Ensembl
Innerchr16:76729187..76729675hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38489
hg19489
hg18489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573136
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)nssv860802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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