A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913936



Internal ID16207892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89887267..90276638hg38UCSC Ensembl
Innerchr2:89926077..90315498hg19UCSC Ensembl
Innerchr2:89563119..89952803hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38389372
hg19389422
hg18389685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582402
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)nssv913936
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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