A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036969



Internal ID92399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73544572..73555762hg38UCSC Ensembl
chr10:75304330..75315520hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3811191
hg1911191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486221
Supporting Variants
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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