A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450669



Internal ID228869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34093226..34099099hg38UCSC Ensembl
chr3:34134718..34140591hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385874
hg195874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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