A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460235



Internal ID238226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:365337..589487hg38UCSC Ensembl
chr5:365452..589602hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38224151
hg19224151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963415
Samples
Known GenesAHRR, C5orf55, EXOC3, MIR4456, PP7080, SLC9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460235
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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