A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027958



Internal ID86334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121889036..121889256hg38UCSC Ensembl
chr9:124651315..124651535hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556662
Supporting Variants
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027958
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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