A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051792



Internal ID102373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134321690..134404260hg38UCSC Ensembl
chr11:134191584..134274154hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3882571
hg1982571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561452
Supporting Variants
Samples
Known GenesB3GAT1, GLB1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051792
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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