A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106540



Internal ID22015773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43469481..43469481hg38UCSC Ensembl
chr22:43865361..43865361hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641919
Samples
Known GenesMPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106540
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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