A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565151



Internal ID16005874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73539224..73545443hg38UCSC Ensembl
Innerchr14:74005928..74012147hg19UCSC Ensembl
Innerchr14:73075681..73081900hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386220
hg196220
hg186220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3771n54
Supporting Variantsnssv829382, nssv829381, nssv829378, nssv829380, nssv829379, nssv829377
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565151
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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