A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266228



Internal ID20833268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123677780..124361191hg38UCSC Ensembl
chr5:123013474..123696884hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38683412
hg19683411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00292


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