A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834394



Internal ID22609329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160676694..160678470hg38UCSC Ensembl
chr3:160394482..160396258hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486519
Samples
Known GenesARL14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834394
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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