A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007671



Internal ID21917014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166449758..166450792hg38UCSC Ensembl
chr6:166863246..166864280hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381035
hg191035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565653
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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