A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722798



Internal ID146464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32091139..32093577hg38UCSC Ensembl
chr19:32582045..32584483hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722798
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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