A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797194



Internal ID19171595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85556121..85601185hg38UCSC Ensembl
Innerchr8:86468350..86513414hg19UCSC Ensembl
Innerchr8:86655602..86700666hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3845065
hg1945065
hg1845065
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891429
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797194
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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