A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239859



Internal ID20806899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11895216..11895837hg38UCSC Ensembl
chr16:11989073..11989694hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577755
Supporting Variants
Samples
Known GenesGSPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239859
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