A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377268



Internal ID22194749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58627424..58631105hg38UCSC Ensembl
chr16:58661328..58665009hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3249141
Supporting Variants
SamplesHG00731
Known GenesCNOT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377268
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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