A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565153



Internal ID16005876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73539224..73556034hg38UCSC Ensembl
Innerchr14:74005928..74022738hg19UCSC Ensembl
Innerchr14:73075681..73092491hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3816811
hg1916811
hg1816811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829393, nssv829394
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565153
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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