A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565151



Internal ID18766227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183734810..183737721hg38UCSC Ensembl
Outerchr4:183734575..183737988hg38UCSC Ensembl
Innerchr4:184655963..184658874hg19UCSC Ensembl
Outerchr4:184655728..184659141hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383414
hg193414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763898
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565151
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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