A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797558



Internal ID19160700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75258014..75318066hg38UCSC Ensembl
Innerchr8:76170249..76230301hg19UCSC Ensembl
Innerchr8:76332804..76392856hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3860053
hg1960053
hg1860053
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891413
Supporting Variants
Samples
Known GenesCASC9
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797558
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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