A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891499



Internal ID19185895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:145013753..145059697hg38UCSC Ensembl
Outerchr8:145013753..145059697hg38UCSC Ensembl
Innerchr8:146239139..146285083hg19UCSC Ensembl
Outerchr8:146239139..146285083hg19UCSC Ensembl
Innerchr8:146209943..146255887hg18UCSC Ensembl
Outerchr8:146209943..146255887hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3845945
hg1945945
hg1845945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788084
Samples
Known GenesC8orf33
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891499
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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