A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706317



Internal ID129983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28330486..28341400hg38UCSC Ensembl
chr16:28341807..28352721hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810915
hg1910915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706317
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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