A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14410182



Internal ID22316692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49972528..49976525hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383998
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201877
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14410182
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