A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484466



Internal ID261877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13633855..13720456hg38UCSC Ensembl
chr9:13633854..13720455hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3886602
hg1986602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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