A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843459



Internal ID22027102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102642303..102642303hg38UCSC Ensembl
chr11:102513034..102513034hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258256
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843459
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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