A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642003



Internal ID21834050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45842055..45842055hg38UCSC Ensembl
chr22:46237935..46237935hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109401
Supporting Variants
Samples
Known GenesATXN10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642003
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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