A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459850



Internal ID237856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159029415..159029696hg38UCSC Ensembl
chr6:159450447..159450728hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459850
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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