A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565034



Internal ID16352443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221751..70222673hg38UCSC Ensembl
Innerchr14:70688468..70689390hg19UCSC Ensembl
Innerchr14:69758221..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38923
hg19923
hg18923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3750n54
Supporting Variantsnssv829058, nssv829055, nssv829061, nssv829057, nssv829067, nssv829059, nssv829056, nssv829063, nssv829062, nssv829066, nssv829054, nssv829068, nssv829065, nssv829064, nssv829060
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565034
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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