A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582762



Internal ID16370171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117026746..117189309hg38UCSC Ensembl
Innerchr2:117784322..117946885hg19UCSC Ensembl
Innerchr2:117500792..117663355hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38162564
hg19162564
hg18162564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7019n54
Supporting Variantsnssv916360
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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