A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563858



Internal ID18764934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53699754..53701256hg38UCSC Ensembl
Outerchr4:53699526..53701615hg38UCSC Ensembl
Innerchr4:54565921..54567423hg19UCSC Ensembl
Outerchr4:54565693..54567782hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762605
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563858
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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