A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746908



Internal ID18721154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93201835..93205455hg38UCSC Ensembl
Outerchr11:93201335..93206334hg38UCSC Ensembl
Innerchr11:92935001..92938621hg19UCSC Ensembl
Outerchr11:92934501..92939500hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746908
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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