A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891489



Internal ID18839199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137456447..138039792hg38UCSC Ensembl
Outerchr8:137456447..138039792hg38UCSC Ensembl
Innerchr8:138468690..139052035hg19UCSC Ensembl
Outerchr8:138468690..139052035hg19UCSC Ensembl
Innerchr8:138537872..139121217hg18UCSC Ensembl
Outerchr8:138537872..139121217hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38583346
hg19583346
hg18583346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791918
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891489
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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