A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269165



Internal ID20836205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350681..6355845hg38UCSC Ensembl
chr5:6350794..6355958hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385165
hg195165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269165
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00196


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