A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687396



Internal ID111062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45312294..45312554hg38UCSC Ensembl
chr13:45886429..45886689hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687396
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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