A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785023



Internal ID19182689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81072446..81108293hg38UCSC Ensembl
Innerchr8:81984681..82020528hg19UCSC Ensembl
Innerchr8:82147236..82183083hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3835848
hg1935848
hg1835848
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891422
Supporting Variants
Samples
Known GenesPAG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785023
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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