A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217631



Internal ID22363225
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14389443, nssv14381844
SamplesHG00731, HG00732
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217631
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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