A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544009



Internal ID20917250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50452079..50485459hg38UCSC Ensembl
chr22:50890508..50923888hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3833381
hg1933381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205731
Samples
Known GenesADM2, SBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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