A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894642



Internal ID22669716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5158181..5163183hg38UCSC Ensembl
chr3:5199866..5204868hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg385003
hg195003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415443
Samples
Known GenesARL8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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