A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796280



Internal ID19165487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6206048..6320781hg38UCSC Ensembl
Innerchr8:6063569..6178302hg19UCSC Ensembl
Innerchr8:6050977..6165710hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38114734
hg19114734
hg18114734
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891307
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=58
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796280
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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