A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618180



Internal ID21810227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81027172..81027172hg38UCSC Ensembl
chr16:81060777..81060777hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080615
Supporting Variants
Samples
Known GenesCENPN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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