A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790887



Internal ID19170977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20863901..20933506hg38UCSC Ensembl
Innerchr8:20721412..20791017hg19UCSC Ensembl
Innerchr8:20765692..20835297hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3869606
hg1969606
hg1869606
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891374
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790887
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer