A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842884



Internal ID22026527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73509141..73509141hg38UCSC Ensembl
chr10:75268899..75268899hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247244
Supporting Variants
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842884
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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