A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022795



Internal ID21932138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79684903..79685098hg38UCSC Ensembl
chr18:77444903..77445098hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619421
Samples
Known GenesCTDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022795
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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