A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547860



Internal ID18748936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60329965..60330445hg38UCSC Ensembl
Outerchr11:60329905..60330557hg38UCSC Ensembl
Innerchr11:60097438..60097918hg19UCSC Ensembl
Outerchr11:60097378..60098030hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746607
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547860
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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