A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707289



Internal ID130955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31326014..31405175hg38UCSC Ensembl
chr16:31337335..31416496hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3879162
hg1979162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519487
Supporting Variants
Samples
Known GenesITGAD, ITGAM, ITGAX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707289
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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