A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466390



Internal ID244231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16272106..16276946hg38UCSC Ensembl
chr5:16272215..16277055hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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