A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478233



Internal ID255796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2746000..2792000hg38UCSC Ensembl
chr9:2746000..2792000hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3846001
hg1946001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478233
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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