A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565775



Internal ID18766851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32797053..32797162hg38UCSC Ensembl
Outerchr5:32797043..32797170hg38UCSC Ensembl
Innerchr5:32797159..32797268hg19UCSC Ensembl
Outerchr5:32797149..32797276hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764522
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565775
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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