A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906914



Internal ID16200870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40972473..41035363hg38UCSC Ensembl
Innerchr2:41199613..41262503hg19UCSC Ensembl
Innerchr2:41053117..41116007hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3862891
hg1962891
hg1862891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581530
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)nssv906914
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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