A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566439



Internal ID18767515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109487922..109490418hg38UCSC Ensembl
Outerchr5:109487773..109490474hg38UCSC Ensembl
Innerchr5:108823623..108826119hg19UCSC Ensembl
Outerchr5:108823474..108826175hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765186
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566439
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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