A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106362



Internal ID22015595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21168400..21326945hg38UCSC Ensembl
chr22:21522689..21681234hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38158546
hg19158546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649472
Samples
Known GenesFAM230B, POM121L8P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106362
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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