A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891484



Internal ID19185880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131437926..131888690hg38UCSC Ensembl
Outerchr8:131437926..131888690hg38UCSC Ensembl
Innerchr8:132450173..132900937hg19UCSC Ensembl
Outerchr8:132450173..132900937hg19UCSC Ensembl
Innerchr8:132519355..132970119hg18UCSC Ensembl
Outerchr8:132519355..132970119hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38450765
hg19450765
hg18450765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792960
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891484
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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