A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024675



Internal ID21934018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24673795..24690391hg38UCSC Ensembl
chr18:22253759..22270355hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3816597
hg1916597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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