A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565036



Internal ID16352445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221772..70222673hg38UCSC Ensembl
Innerchr14:70688489..70689390hg19UCSC Ensembl
Innerchr14:69758242..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38902
hg19902
hg18902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3750n54
Supporting Variantsnssv829070, nssv829072, nssv829071
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565036
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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