A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565147



Internal ID18766223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183464243..183464308hg38UCSC Ensembl
Outerchr4:183464234..183464319hg38UCSC Ensembl
Innerchr4:184385396..184385461hg19UCSC Ensembl
Outerchr4:184385387..184385472hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763894
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565147
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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