A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103892



Internal ID22013125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32491586..32491586hg38UCSC Ensembl
chr22:32887573..32887573hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641433
Samples
Known GenesFBXO7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103892
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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