A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975275



Internal ID50904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159159037..159161264hg38UCSC Ensembl
chr5:158586045..158588272hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466366
Supporting Variants
Samples
Known GenesRNF145
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975275
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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