A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939055



Internal ID26752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152589134..152589370hg38UCSC Ensembl
chr3:152306923..152307159hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05729


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