A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048528



Internal ID100227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76301951..76304193hg38UCSC Ensembl
chr11:76012995..76015237hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382243
hg192243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048528
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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