A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891358



Internal ID19185754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16242771..16410993hg38UCSC Ensembl
Outerchr8:16235147..16439711hg38UCSC Ensembl
Innerchr8:16100280..16268502hg19UCSC Ensembl
Outerchr8:16092656..16297220hg19UCSC Ensembl
Innerchr8:16144651..16312873hg18UCSC Ensembl
Outerchr8:16137027..16341591hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38204565
hg19204565
hg18204565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780816, essv25787709
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891358
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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