A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790905



Internal ID18819271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2489783..2849255hg38UCSC Ensembl
Innerchr8:2346899..2706777hg19UCSC Ensembl
Innerchr8:2334306..2694184hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38359473
hg19359879
hg18359879
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891260
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=137
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790905
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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