A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892010



Internal ID19186406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54944514..55187440hg38UCSC Ensembl
Outerchr11:54944514..55187440hg38UCSC Ensembl
Innerchr11:54711990..54954916hg19UCSC Ensembl
Outerchr11:54711990..54954916hg19UCSC Ensembl
Innerchr11:54468566..54711492hg18UCSC Ensembl
Outerchr11:54468566..54711492hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38242927
hg19242927
hg18242927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790722
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892010
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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