A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3543641



Internal ID22412694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47467226..47780369hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38313144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14458459, nssv14455233
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3543641
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