A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036971



Internal ID92400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73568588..73569906hg38UCSC Ensembl
chr10:75328346..75329664hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381319
hg191319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478597
Supporting Variants
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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