A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891451



Internal ID18839161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100822821..100919373hg38UCSC Ensembl
Outerchr8:100822821..100919373hg38UCSC Ensembl
Innerchr8:101835049..101931601hg19UCSC Ensembl
Outerchr8:101835049..101931601hg19UCSC Ensembl
Innerchr8:101904225..102000777hg18UCSC Ensembl
Outerchr8:101904225..102000777hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3896553
hg1996553
hg1896553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790627
Samples
Known GenesYWHAZ
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891451
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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