A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842563



Internal ID22026206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57620402..57620402hg38UCSC Ensembl
chr11:57387875..57387875hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842563
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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