A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008654



Internal ID7058932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62098895..62139851hg38UCSC Ensembl
Innerchr9:67516297..67557261hg19UCSC Ensembl
Innerchr9:67106117..67147081hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3840957
hg1940965
hg1840965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586299
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008654
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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