A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843270



Internal ID22026913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112338782..112338782hg38UCSC Ensembl
chr11:112209505..112209505hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843270
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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