A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111617



Internal ID21294883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195876092..195925954hg38UCSC Ensembl
Innerchr3:195602963..195652825hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3849863
hg1949863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105502
Samplessample402
Known GenesMIR6829, TNK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111617
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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