A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842793



Internal ID22026436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73164454..73164454hg38UCSC Ensembl
chr11:72875499..72875499hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842793
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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