A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992234



Internal ID7077908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68220553..68254121hg38UCSC Ensembl
Innerchr9:70835469..70869037hg19UCSC Ensembl
Innerchr9:70025289..70058857hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3833569
hg1933569
hg1833569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586541
SamplesHuRef
Known GenesCBWD3, CBWD5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992234
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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