A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877238



Internal ID22652201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20925868..20926100hg38UCSC Ensembl
chr1:21252361..21252593hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359376
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877238
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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