A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105840



Internal ID22015073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46859353..46859353hg38UCSC Ensembl
chr22:47255249..47255249hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639513
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105840
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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