A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837674



Internal ID22612609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133860436..133870206hg38UCSC Ensembl
chr4:134781591..134791361hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg389771
hg199771
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837674
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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