A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3551642



Internal ID22420549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18215202..18357590hg38UCSC Ensembl
chrUn_gl000212:43954..186342hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38142389
hg19142389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459767, nssv14466490, nssv14463050, nssv14458957, nssv14452659, nssv14460129, nssv14465081, nssv14453236, nssv14457134
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3551642
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