A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044202



Internal ID21953491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5160471..5160471hg38UCSC Ensembl
chr3:5202156..5202156hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535505
Samples
Known GenesARL8B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044202
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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