A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069389



Internal ID21978622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39469180..39469180hg38UCSC Ensembl
chr3:39510671..39510671hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537606
Samples
Known GenesMOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069389
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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