A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547993



Internal ID18749069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72263773..72264507hg38UCSC Ensembl
Outerchr11:72263756..72264525hg38UCSC Ensembl
Innerchr11:71974817..71975551hg19UCSC Ensembl
Outerchr11:71974800..71975569hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746740
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547993
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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