A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993276



Internal ID7078609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94515778..94518663hg38UCSC Ensembl
Innerchr11:94248944..94251829hg19UCSC Ensembl
Innerchr11:93888592..93891477hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382886
hg192886
hg182886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586201
SamplesHuRef
Known GenesLOC643037
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993276
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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