A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931578



Internal ID21793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40768468..40768474hg38UCSC Ensembl
chr3:40809959..40809965hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931578
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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