A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843866



Internal ID22027509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45738813..45738813hg38UCSC Ensembl
chr12:46132596..46132596hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240987
Supporting Variants
Samples
Known GenesARID2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843866
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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