A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058524



Internal ID21967757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23161680..23161743hg38UCSC Ensembl
chr20:23142317..23142380hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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