A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704745



Internal ID128411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20711811..20713797hg38UCSC Ensembl
chr16:20723133..20725119hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381987
hg191987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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