A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625172



Internal ID21817219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22231951..22232857hg38UCSC Ensembl
chr18:19811914..19812820hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625172
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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