A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892053



Internal ID19186449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87897040..88103616hg38UCSC Ensembl
Outerchr11:87897040..88103616hg38UCSC Ensembl
Innerchr11:87607932..87836784hg19UCSC Ensembl
Outerchr11:87607932..87836784hg19UCSC Ensembl
Innerchr11:87285580..87476432hg18UCSC Ensembl
Outerchr11:87285580..87476432hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38206577
hg19228853
hg18190853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787659
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892053
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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