A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891463



Internal ID19185859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114514291..114851271hg38UCSC Ensembl
Outerchr8:114514291..114851271hg38UCSC Ensembl
Innerchr8:115526520..115863500hg19UCSC Ensembl
Outerchr8:115526520..115863500hg19UCSC Ensembl
Innerchr8:115595696..115932676hg18UCSC Ensembl
Outerchr8:115595696..115932676hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38336981
hg19336981
hg18336981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780970
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891463
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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