A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223151



Internal ID22367006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89567507..89567574hg38UCSC Ensembl
chr14:90033851..90033918hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2713n152
Supporting Variantsnssv14384767, nssv14377023, nssv14388905
SamplesNA19238, NA19239, NA19240
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223151
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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