A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923178



Internal ID22698404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133382590..133382847hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923178
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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