A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547865



Internal ID18748941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60804006..60804424hg38UCSC Ensembl
Outerchr11:60803938..60804571hg38UCSC Ensembl
Innerchr11:60571479..60571897hg19UCSC Ensembl
Outerchr11:60571411..60572044hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746612
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547865
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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