A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452890



Internal ID231032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166243692..166314270hg38UCSC Ensembl
chr3:165961480..166032058hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3870579
hg1970579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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