A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709441



Internal ID133107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56972495..56972546hg38UCSC Ensembl
chr16:57006407..57006458hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg386010
hg196010
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563345
Supporting Variants
Samples
Known GenesCETP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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