A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943628



Internal ID29732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177922860..177929485hg38UCSC Ensembl
chr3:177640648..177647273hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943628
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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