A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891408



Internal ID18839118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:68274041..68368132hg38UCSC Ensembl
Outerchr8:68273291..68383349hg38UCSC Ensembl
Innerchr8:69186276..69280367hg19UCSC Ensembl
Outerchr8:69185526..69295584hg19UCSC Ensembl
Innerchr8:69348830..69442921hg18UCSC Ensembl
Outerchr8:69348080..69458138hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38110059
hg19110059
hg18110059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789874, essv25790285, essv25788717
Samples
Known GenesC8orf34, LOC286189
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891408
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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