A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064234



Internal ID21973467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45393719..45393719hg38UCSC Ensembl
chr3:45435211..45435211hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538851
Samples
Known GenesLARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064234
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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