A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564139



Internal ID16351548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27885392..27989467hg38UCSC Ensembl
Innerchr14:28354598..28458673hg19UCSC Ensembl
Innerchr14:27424438..27528513hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38104076
hg19104076
hg18104076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3596n54
Supporting Variantsnssv825078
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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