A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454208



Internal ID21111761
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 StatusM
Merged Variants
Supporting Variantsnssv18233640
Samples
Known GenesZBTB26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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