A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092380



Internal ID22001613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108215435..108215435hg38UCSC Ensembl
chr13:108867783..108867783hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608927
Samples
Known GenesLIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092380
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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