A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719075



Internal ID18670670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79171946..79205069hg38UCSC Ensembl
Innerchr16:79205843..79238966hg19UCSC Ensembl
Innerchr16:77763344..77796467hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3833124
hg1933124
hg1833124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060491
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719075
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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