A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084718



Internal ID21993951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24613499..24613499hg38UCSC Ensembl
chr16:24624820..24624820hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084718
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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