A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260782



Internal ID20827822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51433512..51433958hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260782
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