A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2802184



Internal ID15678121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73528471..73528999hg38UCSC Ensembl
Innerchr14:73995175..73995703hg19UCSC Ensembl
Innerchr14:73064928..73065456hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38529
hg19529
hg18529
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514745
Supporting Variants
SamplesNA18564
Known GenesHEATR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2802184
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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