A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632508



Internal ID21824555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23009123..23009123hg38UCSC Ensembl
chr20:22989760..22989760hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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