A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480094



Internal ID257605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132883703..132884881hg38UCSC Ensembl
chr9:135759090..135760268hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030024
Samples
Known GenesC9orf9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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