A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080572



Internal ID21989805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54378372..54378372hg38UCSC Ensembl
chr16:54412284..54412284hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080572
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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