A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939164



Internal ID26827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129389269..129389416hg38UCSC Ensembl
chr3:129108112..129108259hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448464
Supporting Variants
Samples
Known GenesRPL32P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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