A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117409



Internal ID21300675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133861156..133879644hg38UCSC Ensembl
Innerchr4:134782311..134800799hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3818489
hg1918489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090456
Samplessample148
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117409
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