A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052483



Internal ID102836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113821142..113821217hg38UCSC Ensembl
chr11:113691864..113691939hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507126
Supporting Variants
Samples
Known GenesUSP28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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