A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586051



Internal ID6710747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61855390..62087447hg38UCSC Ensembl
Innerchr9:44991542..45223599hg19UCSC Ensembl
Innerchr9:44931538..45163595hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38232058
hg19232058
hg18232058
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007212
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586051
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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