A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14446390



Internal ID22224946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18507465..18507519hg38UCSC Ensembl
chr16:14982363..14982417hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207344
Supporting Variants
SamplesHG00733
Known GenesNOMO1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14446390
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