A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705380



Internal ID129046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2903403..2903548hg38UCSC Ensembl
chr16:2953404..2953549hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705380
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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