A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060437



Internal ID21969671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40228305..40228379hg38UCSC Ensembl
chr22:40624309..40624383hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648357
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060437
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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