A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551374



Internal ID20924510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49757827..49778753hg38UCSC Ensembl
chr22:50151475..50172401hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3820927
hg1920927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205708
Samples
Known GenesBRD1, LOC90834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551374
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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