A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483399



Internal ID260834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85955040..85955266hg38UCSC Ensembl
chr9:88569955..88570181hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025577
Samples
Known GenesNAA35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483399
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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