A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937894



Internal ID25977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391212..107391290hg38UCSC Ensembl
chr3:107110059..107110137hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.498438


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