A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101397



Internal ID22010630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46860144..46860144hg38UCSC Ensembl
chr22:47256040..47256040hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641735
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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