A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436031



Internal ID214658
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 StatusM
Merged Variants
Supporting Variantsnssv16944093
Samples
Known GenesIL1RAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436031
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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