A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764563



Internal ID18738809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36485983..36486195hg38UCSC Ensembl
Outerchr5:36485929..36486209hg38UCSC Ensembl
Innerchr5:36486085..36486297hg19UCSC Ensembl
Outerchr5:36486031..36486311hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764563
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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