A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586299



Internal ID7057681
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008654
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586299
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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