A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746933



Internal ID18721179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95436288..95442185hg38UCSC Ensembl
Outerchr11:95436143..95442393hg38UCSC Ensembl
Innerchr11:95169452..95175349hg19UCSC Ensembl
Outerchr11:95169307..95175557hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386251
hg196251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746933
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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