A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3545410



Internal ID22414420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:370390..370390hg38UCSC Ensembl
chr16:420390..420390hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445852
SamplesHG00733
Known GenesMRPL28
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3545410
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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