A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944093



Internal ID30056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190631901..190632064hg38UCSC Ensembl
chr3:190349690..190349853hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436031
Supporting Variants
Samples
Known GenesIL1RAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007649


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