A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114299



Internal ID21297565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184432124..184434060hg38UCSC Ensembl
Innerchr4:185353278..185355214hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381937
hg191937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093361
Samplessample275
Known GenesIRF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114299
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