A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934633



Internal ID23823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59520531..59537613hg38UCSC Ensembl
chr3:59506257..59523339hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3817083
hg1917083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934633
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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