A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933823



Internal ID16227779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240161493..240213008hg38UCSC Ensembl
Innerchr2:241100910..241152425hg19UCSC Ensembl
Innerchr2:240749583..240801098hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3851516
hg1951516
hg1851516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584803
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933823
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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