A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932943



Internal ID22686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47267827..47267885hg38UCSC Ensembl
chr3:47309317..47309375hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439274
Supporting Variants
Samples
Known GenesKIF9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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