A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266960



Internal ID20834000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68043591..68044719hg38UCSC Ensembl
chr5:67339419..67340547hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266960
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