A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2823879



Internal ID15713796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72056488..72059896hg38UCSC Ensembl
Innerchr16:72090387..72093795hg19UCSC Ensembl
Innerchr16:70647888..70651296hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg383409
hg193409
hg183409
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514812
Supporting Variants
SamplesNA18967
Known GenesHP
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2823879
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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