A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460259



Internal ID238250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32207422..32207589hg38UCSC Ensembl
chr5:32207528..32207695hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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