A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115975



Internal ID21299241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119032843..119056490hg38UCSC Ensembl
Innerchr6:119354008..119377655hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3823648
hg1923648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083582
Samplessample37
Known GenesFAM184A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115975
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