A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792300



Internal ID19168453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163617018..164017426hg38UCSC Ensembl
Innerchr3:163334806..163735214hg19UCSC Ensembl
Innerchr3:164817500..165217908hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38400409
hg19400409
hg18400409
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893804
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=89
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792300
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