A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829369



Internal ID15776639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534434..73557222hg38UCSC Ensembl
Innerchr14:74001138..74023926hg19UCSC Ensembl
Innerchr14:73070891..73093679hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3822789
hg1922789
hg1822789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565145
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)nssv829369
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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