A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246460



Internal ID22051070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183320860..183320860hg38UCSC Ensembl
chr1:183289995..183289995hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17840177
Samples
Known GenesNMNAT2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246460
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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