A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065698



Internal ID21974931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134538531..134538531hg38UCSC Ensembl
chr3:134257373..134257373hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540244
Samples
Known GenesCEP63
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065698
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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