A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746649



Internal ID18720895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64725135..64725343hg38UCSC Ensembl
Outerchr11:64725124..64725377hg38UCSC Ensembl
Innerchr11:64492607..64492815hg19UCSC Ensembl
Outerchr11:64492596..64492849hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746649
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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