A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620029



Internal ID21812076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27279861..27282261hg38UCSC Ensembl
chr18:24859825..24862225hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620029
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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