A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913937



Internal ID16207893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89898914..90229639hg38UCSC Ensembl
Innerchr2:89937724..90268505hg19UCSC Ensembl
Innerchr2:89574766..89905810hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38330726
hg19330782
hg18331045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582403
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)nssv913937
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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