A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560489



Internal ID21884844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22643661..22643661hg38UCSC Ensembl
chr6:22643890..22643890hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560489
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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