A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205708



Internal ID20772748
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 StatusS
Merged Variantsnsv6551374
Supporting Variants
Samples
Known GenesBRD1, LOC90834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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