A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573261



Internal ID16360670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78616923..78700014hg38UCSC Ensembl
Innerchr16:78650820..78733911hg19UCSC Ensembl
Innerchr16:77208321..77291412hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3883092
hg1983092
hg1883092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861607
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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