A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706577



Internal ID130243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24695739..24698464hg38UCSC Ensembl
chr16:24707060..24709785hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382726
hg192726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706577
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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