A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036965



Internal ID92398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73509654..73509748hg38UCSC Ensembl
chr10:75269412..75269506hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485966
Supporting Variants
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036965
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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