A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891458



Internal ID19185854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110327150..110501171hg38UCSC Ensembl
Outerchr8:110327150..110501171hg38UCSC Ensembl
Innerchr8:111339379..111513400hg19UCSC Ensembl
Outerchr8:111339379..111513400hg19UCSC Ensembl
Innerchr8:111408555..111582576hg18UCSC Ensembl
Outerchr8:111408555..111582576hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38174022
hg19174022
hg18174022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799506
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891458
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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