A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114446



Internal ID21297712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25034095..25037451hg38UCSC Ensembl
Innerchr18:22614059..22617415hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383357
hg193357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099494
Samplessample78
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114446
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