A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv923513



Internal ID15870783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:160107092..160222924hg38UCSC Ensembl
Innerchr2:160963603..161079435hg19UCSC Ensembl
Innerchr2:160671849..160787681hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38115833
hg19115833
hg18115833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583497
Supporting Variants
Samples
Known GenesITGB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv923513
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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