A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891413



Internal ID19185809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75258014..75318066hg38UCSC Ensembl
Outerchr8:75258014..75318066hg38UCSC Ensembl
Innerchr8:76170249..76230301hg19UCSC Ensembl
Outerchr8:76170249..76230301hg19UCSC Ensembl
Innerchr8:76332804..76392856hg18UCSC Ensembl
Outerchr8:76332804..76392856hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3860053
hg1960053
hg1860053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797558
Samples
Known GenesCASC9
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891413
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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