A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050840



Internal ID101774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90028896..90094896hg38UCSC Ensembl
chr11:89762064..89828064hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3866001
hg1966001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143326
Supporting Variants
Samples
Known GenesTRIM49C, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.095487


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