A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755137



Internal ID18729383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40117271..40119390hg38UCSC Ensembl
Outerchr19:40117149..40119408hg38UCSC Ensembl
Innerchr19:40623178..40625297hg19UCSC Ensembl
Outerchr19:40623056..40625315hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755137
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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