A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060782



Internal ID21970015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86524864..86524864hg38UCSC Ensembl
chr8:87537092..87537092hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590022
Samples
Known GenesCPNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060782
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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