A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381844



Internal ID22209526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89207628..89213738hg38UCSC Ensembl
chr14:89673972..89680082hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217631
Supporting Variants
SamplesHG00732
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381844
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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