A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069091



Internal ID21978324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83050823..83050823hg38UCSC Ensembl
chr6:83760542..83760542hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561698
Samples
Known GenesUBE3D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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