A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746707



Internal ID18720953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69759198..69759256hg38UCSC Ensembl
chr11:69573966..69574024hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746707
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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