A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065289



Internal ID21974522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65590694..65590694hg38UCSC Ensembl
chr5:64886521..64886521hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545722
Samples
Known GenesTRIM23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065289
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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