A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011868



Internal ID21921211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127584744..127592661hg38UCSC Ensembl
chr6:127905889..127913806hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg387918
hg197918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561766
Samples
Known GenesC6orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011868
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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