A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459546



Internal ID237559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13202795..13338445hg38UCSC Ensembl
chr5:13202907..13338557hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38135651
hg19135651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459546
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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