A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844069



Internal ID22027712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66015376..66015376hg38UCSC Ensembl
chr12:66409156..66409156hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844069
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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