A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446778



Internal ID225096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188940444..188940526hg38UCSC Ensembl
chr3:188658233..188658315hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446778
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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