A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2792061



Internal ID15362290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43026600..43028940hg38UCSC Ensembl
Innerchr13:43600736..43603076hg19UCSC Ensembl
Innerchr13:42498736..42501076hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382341
hg192341
hg182341
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514696
Supporting Variants
SamplesNA18949
Known GenesDNAJC15
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2792061
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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