A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825080



Internal ID16119036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27885392..27996354hg38UCSC Ensembl
Innerchr14:28354598..28465560hg19UCSC Ensembl
Innerchr14:27424438..27535402hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38110963
hg19110963
hg18110965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564140
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)nssv825080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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