A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052322



Internal ID102729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120129631..120131723hg38UCSC Ensembl
chr11:120000339..120002431hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507004
Supporting Variants
Samples
Known GenesTRIM29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052322
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002185


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