A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088417



Internal ID21267190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124251317..124299768hg38UCSC Ensembl
Innerchr9:127013596..127062047hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3848452
hg1948452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113986
Supporting Variants
Samplessample11
Known GenesNEK6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088417
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