A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438370



Internal ID216936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33455093..33455163hg38UCSC Ensembl
chr3:33496585..33496655hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438370
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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