A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891464



Internal ID19185860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114591430..114630179hg38UCSC Ensembl
Outerchr8:114591430..114630179hg38UCSC Ensembl
Innerchr8:115603659..115642408hg19UCSC Ensembl
Outerchr8:115603659..115642408hg19UCSC Ensembl
Innerchr8:115672835..115711584hg18UCSC Ensembl
Outerchr8:115672835..115711584hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3838750
hg1938750
hg1838750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797666
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891464
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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