A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992205



Internal ID7077879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32882753..32883307hg38UCSC Ensembl
Innerchr9:32882751..32883305hg19UCSC Ensembl
Innerchr9:32872751..32873305hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586307
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992205
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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