A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001878



Internal ID7066997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44724007..44724467hg38UCSC Ensembl
Innerchr20:43352648..43353108hg19UCSC Ensembl
Innerchr20:42786062..42786522hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38461
hg19461
hg18461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587056
SamplesHuRef
Known GenesWISP2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001878
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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