A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080368



Internal ID21989601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79221877..79221877hg38UCSC Ensembl
chr6:79931594..79931594hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574915
Samples
Known GenesHMGN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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