A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084193



Internal ID21993426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38925484..38925484hg38UCSC Ensembl
chr13:39499621..39499621hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084193
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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