A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827512



Internal ID16121468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43021729..43081995hg38UCSC Ensembl
Innerchr14:43490932..43551198hg19UCSC Ensembl
Innerchr14:42560682..42620948hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3860267
hg1960267
hg1860267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564627
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)nssv827512
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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