A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548113



Internal ID18749189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88361545..88361899hg38UCSC Ensembl
Outerchr11:88361501..88361912hg38UCSC Ensembl
Innerchr11:88094713..88095067hg19UCSC Ensembl
Outerchr11:88094669..88095080hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746860
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548113
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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