A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272389



Internal ID20481607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58354540..58354540hg38UCSC Ensembl
chr16:58388444..58388444hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385927
hg195927
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272389
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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