A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462596



Internal ID240523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33517167..33525994hg38UCSC Ensembl
chr5:33517272..33526099hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388828
hg198828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462596
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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