A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069474



Internal ID21978707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132718933..132718933hg38UCSC Ensembl
chr5:132054625..132054625hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555248
Samples
Known GenesKIF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069474
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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