A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742384



Internal ID18716630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:71639187..71639498hg38UCSC Ensembl
Outerchr8:71639115..71639570hg38UCSC Ensembl
Innerchr8:72551422..72551733hg19UCSC Ensembl
Outerchr8:72551350..72551805hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742384
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer