A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114468



Internal ID21297734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65142459..65143403hg38UCSC Ensembl
Innerchr16:65176362..65177306hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n145
Supporting Variantsnssv14098350
Samplessample75
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114468
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