A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065692



Internal ID21974925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153022885..153022885hg38UCSC Ensembl
chr3:152740674..152740674hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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