A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080259



Internal ID21989492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20024071..20024071hg38UCSC Ensembl
chr6:20024302..20024302hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080259
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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