A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068042



Internal ID21977275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153478531..153478531hg38UCSC Ensembl
chr3:153196320..153196320hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068042
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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