A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051732



Internal ID102329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133555223..133555871hg38UCSC Ensembl
chr11:133425118..133425766hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051732
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer