A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248343



Internal ID20815383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37724231..37724689hg38UCSC Ensembl
chr19:38215132..38215590hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248343
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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