A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891483



Internal ID19185879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129099922..129118358hg38UCSC Ensembl
Outerchr8:129099922..129118358hg38UCSC Ensembl
Innerchr8:130112168..130130604hg19UCSC Ensembl
Outerchr8:130112168..130130604hg19UCSC Ensembl
Innerchr8:130181350..130199786hg18UCSC Ensembl
Outerchr8:130181350..130199786hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3818437
hg1918437
hg1818437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784948
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891483
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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