A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018389



Internal ID21927732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79464218..79464809hg38UCSC Ensembl
chr8:80376453..80377044hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018389
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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