A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586156



Internal ID7057538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38379010..38379847hg38UCSC Ensembl
Innerchr9:38379007..38379844hg19UCSC Ensembl
Innerchr9:38369007..38369844hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004008
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586156
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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