A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217157



Internal ID20784197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133382579..133382740hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00089


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