A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358180



Internal ID21015733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5101802..5128214hg38UCSC Ensembl
chr3:5143487..5169899hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3826413
hg1926413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209383
Samples
Known GenesARL8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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