A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451087



Internal ID229273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146357387..146365937hg38UCSC Ensembl
chr3:146075174..146083724hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg388551
hg198551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451087
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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