A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901954



Internal ID22677107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190631907..190632043hg38UCSC Ensembl
chr3:190349696..190349832hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417819
Samples
Known GenesIL1RAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901954
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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