A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916360



Internal ID16210316
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 StatusS
Merged Variantsnsv582762
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)nssv916360
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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