A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458786



Internal ID236807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146716195..146716355hg38UCSC Ensembl
chr5:146095758..146095918hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974678
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458786
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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