A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268254



Internal ID20835294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181119818..181229597hg38UCSC Ensembl
chr5:180546818..180656597hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38109780
hg19109780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559883
Supporting Variants
Samples
Known GenesLOC102577426, MIR4638, OR2V1, OR2V2, TRIM41, TRIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268254
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