A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086467



Internal ID21995700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98437709..98437709hg38UCSC Ensembl
chr15:98980938..98980938hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604212
Samples
Known GenesFAM169B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086467
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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