A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564563



Internal ID16351972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42008053..42175414hg38UCSC Ensembl
Innerchr14:42477256..42644617hg19UCSC Ensembl
Innerchr14:41547006..41714367hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38167362
hg19167362
hg18167362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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