A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563788



Internal ID18764864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43682584..43682747hg38UCSC Ensembl
Outerchr4:43682579..43682785hg38UCSC Ensembl
Innerchr4:43684601..43684764hg19UCSC Ensembl
Outerchr4:43684596..43684802hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762535
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563788
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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