A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563911



Internal ID18764987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58741440..58741722hg38UCSC Ensembl
Outerchr4:58741391..58741786hg38UCSC Ensembl
Innerchr4:59607605..59607887hg19UCSC Ensembl
Outerchr4:59607556..59607951hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762658
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563911
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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