A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851389



Internal ID22035032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10947157..10947157hg38UCSC Ensembl
chrUn_gl000241:22585..22585hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251942
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851389
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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