A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891404



Internal ID19185800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:59121869..59181395hg38UCSC Ensembl
Outerchr8:59121869..59181395hg38UCSC Ensembl
Innerchr8:60034428..60093954hg19UCSC Ensembl
Outerchr8:60034428..60093954hg19UCSC Ensembl
Innerchr8:60196982..60256508hg18UCSC Ensembl
Outerchr8:60196982..60256508hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3859527
hg1959527
hg1859527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792937
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891404
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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