A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548163



Internal ID18749239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93287326..93295834hg38UCSC Ensembl
Outerchr11:93285835..93296857hg38UCSC Ensembl
Innerchr11:93020492..93029000hg19UCSC Ensembl
Outerchr11:93019001..93030023hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811023
hg1911023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746910
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548163
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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