A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022399



Internal ID21931742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50203053..50224142hg38UCSC Ensembl
chr18:47729423..47750512hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3821090
hg1921090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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