A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954879



Internal ID37234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108552466..108552541hg38UCSC Ensembl
chr4:109473622..109473697hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473777
Supporting Variants
Samples
Known GenesRPL34-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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