A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2862587



Internal ID15397292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45723235..45724003hg38UCSC Ensembl
Innerchr20:44351874..44352642hg19UCSC Ensembl
Innerchr20:43785288..43786056hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514940
Supporting Variants
SamplesNA19146
Known GenesSPINT4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2862587
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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