A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913803



Internal ID16207759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81960228..82093530hg38UCSC Ensembl
Innerchr2:82187352..82320654hg19UCSC Ensembl
Innerchr2:82040863..82174165hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38133303
hg19133303
hg18133303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582346
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)nssv913803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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