A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089366



Internal ID21998599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38345031..38345031hg38UCSC Ensembl
chr13:38919168..38919168hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382544
hg192544
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089366
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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