A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233640



Internal ID20800680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122926058..122928068hg38UCSC Ensembl
chr9:125688337..125690347hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454208
Supporting Variants
Samples
Known GenesZBTB26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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