A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742349



Internal ID18716595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:65863478..65864543hg38UCSC Ensembl
Outerchr8:65863431..65864624hg38UCSC Ensembl
Innerchr8:66775713..66776778hg19UCSC Ensembl
Outerchr8:66775666..66776859hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543602
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742349
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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