A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564119



Internal ID16351528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27067046..27305738hg38UCSC Ensembl
Innerchr14:27536252..27774944hg19UCSC Ensembl
Innerchr14:26606092..26844784hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38238693
hg19238693
hg18238693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825062
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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