A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099798



Internal ID22009031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45931107..45931107hg38UCSC Ensembl
chr13:46505242..46505242hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099798
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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