A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114321



Internal ID21297587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78794730..78808221hg38UCSC Ensembl
Innerchr18:76554730..76568221hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3813492
hg1913492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100244
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114321
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