A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114990



Internal ID21298256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89038313..89072832hg38UCSC Ensembl
Innerchr8:90050542..90085061hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3834520
hg1934520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087174
Samplessample133
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114990
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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