A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022769



Internal ID21932112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86121586..86121940hg38UCSC Ensembl
chr16:86155192..86155546hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022769
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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