A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727292



Internal ID150958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46185840..46187086hg38UCSC Ensembl
chr21:47605754..47607000hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727292
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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