A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445878



Internal ID224216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143175172..143243042hg38UCSC Ensembl
chr3:142894014..142961884hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3867871
hg1967871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445878
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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