A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409151



Internal ID188473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73569947..73569953hg38UCSC Ensembl
chr10:75329705..75329711hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036972
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409151
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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