A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084087



Internal ID21993320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28266748..28266748hg38UCSC Ensembl
chr16:28278069..28278069hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384065
hg194065
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084087
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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