A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547413



Internal ID18748489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20547849..20549579hg38UCSC Ensembl
Outerchr11:20547601..20549883hg38UCSC Ensembl
Innerchr11:20569395..20571125hg19UCSC Ensembl
Outerchr11:20569147..20571429hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746160
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547413
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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