A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239280



Internal ID20806321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55205207..55209730hg38UCSC Ensembl
chr16:55239119..55243642hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg384524
hg194524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239280
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