A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459262



Internal ID237279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145478626..145479366hg38UCSC Ensembl
chr5:144858189..144858929hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459262
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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