A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891374



Internal ID19185770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20863901..20933506hg38UCSC Ensembl
Outerchr8:20863901..20933506hg38UCSC Ensembl
Innerchr8:20721412..20791017hg19UCSC Ensembl
Outerchr8:20721412..20791017hg19UCSC Ensembl
Innerchr8:20765692..20835297hg18UCSC Ensembl
Outerchr8:20765692..20835297hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3869606
hg1969606
hg1869606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790887
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891374
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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