A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547849



Internal ID18748925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58453152..58453456hg38UCSC Ensembl
Outerchr11:58453087..58453488hg38UCSC Ensembl
Innerchr11:58220625..58220929hg19UCSC Ensembl
Outerchr11:58220560..58220961hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746596
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547849
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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