A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3551069



Internal ID22419985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57777902..58068779hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38290878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459478, nssv14460956
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3551069
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