A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565149



Internal ID18766225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183533540..183534678hg38UCSC Ensembl
Outerchr4:183533527..183534690hg38UCSC Ensembl
Innerchr4:184454693..184455831hg19UCSC Ensembl
Outerchr4:184454680..184455843hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763896
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565149
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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