A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933664



Internal ID23175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44820370..44838166hg38UCSC Ensembl
chr3:44861862..44879658hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3817797
hg1917797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450282
Supporting Variants
Samples
Known GenesKIF15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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