A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730632



Internal ID154298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6879054..6879471hg38UCSC Ensembl
chr20:6859701..6860118hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730632
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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