A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478443



Internal ID255997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92168218..92191457hg38UCSC Ensembl
chr9:94930500..94953739hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3823240
hg1923240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478443
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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