A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563909



Internal ID18764985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58563482..58568469hg38UCSC Ensembl
Outerchr4:58562679..58569414hg38UCSC Ensembl
Innerchr4:59429647..59434634hg19UCSC Ensembl
Outerchr4:59428844..59435579hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762656
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563909
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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