A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564117



Internal ID16351526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27039536..27117363hg38UCSC Ensembl
Innerchr14:27508742..27586569hg19UCSC Ensembl
Innerchr14:26578582..26656409hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3877828
hg1977828
hg1877828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3592n54
Supporting Variantsnssv825060
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564117
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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