A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742494



Internal ID18716740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82090349..82093159hg38UCSC Ensembl
Outerchr8:82090270..82093376hg38UCSC Ensembl
Innerchr8:83002584..83005394hg19UCSC Ensembl
Outerchr8:83002505..83005611hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383107
hg193107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543747
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742494
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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