A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233014



Internal ID20800054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65540201..65579400hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3839200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0045


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