A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891473



Internal ID19185869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119317700..119351734hg38UCSC Ensembl
Outerchr8:119317700..119351734hg38UCSC Ensembl
Innerchr8:120329940..120363974hg19UCSC Ensembl
Outerchr8:120329940..120363974hg19UCSC Ensembl
Innerchr8:120399121..120433155hg18UCSC Ensembl
Outerchr8:120399121..120433155hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3834035
hg1934035
hg1834035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786888
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891473
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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