A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989344



Internal ID6725314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:291680..292918hg38UCSC Ensembl
Innerchr11:291680..292918hg19UCSC Ensembl
Innerchr11:281680..282918hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381239
hg191239
hg181239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587028
SamplesHuRef
Known GenesATHL1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989344
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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