A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473777



Internal ID251459
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 StatusM
Merged Variants
Supporting Variantsnssv16954879
Samples
Known GenesRPL34-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473777
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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