A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573133



Internal ID16013856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78078366..78181055hg38UCSC Ensembl
Innerchr16:78112263..78214952hg19UCSC Ensembl
Innerchr16:76669764..76772453hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38102690
hg19102690
hg18102690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv860795
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573133
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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