A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843264



Internal ID22026907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111981087..111981087hg38UCSC Ensembl
chr11:111851812..111851812hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258342
Supporting Variants
Samples
Known GenesDIXDC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843264
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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