A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548465



Internal ID18749541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124905540..124908104hg38UCSC Ensembl
Outerchr11:124905055..124908501hg38UCSC Ensembl
Innerchr11:124775436..124778000hg19UCSC Ensembl
Outerchr11:124774951..124778397hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383447
hg193447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747212
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548465
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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