A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111909



Internal ID21295175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165785067..165788785hg38UCSC Ensembl
Innerchr1:165754304..165758022hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg383719
hg193719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103030
Samplessample4
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111909
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