A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709391



Internal ID133057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47877525..47878047hg38UCSC Ensembl
chr16:47911436..47911958hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709391
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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