A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850726



Internal ID22034369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32342709..32342709hg38UCSC Ensembl
chr21:33715018..33715018hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251848
Supporting Variants
Samples
Known GenesURB1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850726
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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