A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891422



Internal ID19185818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81072446..81108293hg38UCSC Ensembl
Outerchr8:81072446..81108293hg38UCSC Ensembl
Innerchr8:81984681..82020528hg19UCSC Ensembl
Outerchr8:81984681..82020528hg19UCSC Ensembl
Innerchr8:82147236..82183083hg18UCSC Ensembl
Outerchr8:82147236..82183083hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3835848
hg1935848
hg1835848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785023, essv25798671
Samples
Known GenesPAG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891422
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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