A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933761



Internal ID23242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48724164..48724883hg38UCSC Ensembl
chr3:48761597..48762316hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933761
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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