A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547676



Internal ID18748752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44091960..44093753hg38UCSC Ensembl
Outerchr11:44091940..44093759hg38UCSC Ensembl
Innerchr11:44113510..44115303hg19UCSC Ensembl
Outerchr11:44113490..44115309hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381820
hg191820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746423
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547676
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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