A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116933



Internal ID21300199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33788774..34089444hg38UCSC Ensembl
Innerchr16:33591241..33891911hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38300671
hg19300671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv437n145
Supporting Variantsnssv14099106, nssv14097904
Samplessample402, sample137
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116933
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer