A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891460



Internal ID19185856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113782341..114071908hg38UCSC Ensembl
Outerchr8:113782341..114071908hg38UCSC Ensembl
Innerchr8:114794570..115084137hg19UCSC Ensembl
Outerchr8:114794570..115084137hg19UCSC Ensembl
Innerchr8:114863746..115153313hg18UCSC Ensembl
Outerchr8:114863746..115153313hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38289568
hg19289568
hg18289568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784688
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891460
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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