A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829299



Internal ID15776569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73527984..73539437hg38UCSC Ensembl
Innerchr14:73994688..74006141hg19UCSC Ensembl
Innerchr14:73064441..73075894hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3811454
hg1911454
hg1811454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565110
Supporting Variants
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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