A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111406



Internal ID21294672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53721222..53732344hg38UCSC Ensembl
Innerchr16:53755134..53766256hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3811123
hg1911123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098300
Samplessample51
Known GenesFTO
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111406
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