A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586293



Internal ID6710989
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996891
Supporting Variants
SamplesHuRef
Known GenesFAM27E1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586293
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer