A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586736



Internal ID7058118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70000513..70006328hg38UCSC Ensembl
Innerchr11:69846619..69852434hg19UCSC Ensembl
Innerchr11:69524267..69530082hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385816
hg195816
hg185816
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994600
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586736
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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