A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996891



Internal ID6732833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67608563..67723813hg38UCSC Ensembl
Innerchr9:46266431..46391053hg19UCSC Ensembl
Innerchr9:46156427..46281049hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38115251
hg19124623
hg18124623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586293
SamplesHuRef
Known GenesFAM27E1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996891
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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