A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966379



Internal ID44907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32885440..32886557hg38UCSC Ensembl
chr5:32885546..32886663hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966379
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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