A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548496



Internal ID18749572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127815706..127816137hg38UCSC Ensembl
Outerchr11:127815670..127816240hg38UCSC Ensembl
Innerchr11:127685601..127686032hg19UCSC Ensembl
Outerchr11:127685565..127686135hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747243
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548496
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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