A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019120



Internal ID21928463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123070189..123074042hg38UCSC Ensembl
chr8:124082429..124086282hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383854
hg193854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588396
Samples
Known GenesTBC1D31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019120
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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