A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646239



Internal ID21838286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45031746..45031746hg38UCSC Ensembl
chr22:45427627..45427627hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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