A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937752



Internal ID25878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133382795..133382949hg38UCSC Ensembl
chr3:133101639..133101793hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439394
Supporting Variants
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937752
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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