A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891411



Internal ID19185807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75286004..75315259hg38UCSC Ensembl
Outerchr8:75286004..75315259hg38UCSC Ensembl
Innerchr8:76198239..76227494hg19UCSC Ensembl
Outerchr8:76198239..76227494hg19UCSC Ensembl
Innerchr8:76360794..76390049hg18UCSC Ensembl
Outerchr8:76360794..76390049hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3829256
hg1929256
hg1829256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784106, essv25785253
Samples
Known GenesCASC9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891411
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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