A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560550



Internal ID22429347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89204983..89204983hg38UCSC Ensembl
chr14:89671327..89671327hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14391113, nssv14379754, nssv14391628
SamplesNA19238, NA19239, NA19240
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560550
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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