A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548072



Internal ID18749148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83126959..83135059hg38UCSC Ensembl
Outerchr11:83126330..83136458hg38UCSC Ensembl
Innerchr11:82838001..82846101hg19UCSC Ensembl
Outerchr11:82837372..82847500hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3810129
hg1910129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746819
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548072
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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