A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094065



Internal ID22003298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79624943..79624943hg38UCSC Ensembl
chr13:80199078..80199078hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094065
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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