A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843206



Internal ID22026849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41958161..41958161hg38UCSC Ensembl
chr12:42351963..42351963hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843206
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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