A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586307



Internal ID7057689
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992205
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586307
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