A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241308



Internal ID22045918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232749611..232749611hg38UCSC Ensembl
chr1:232885357..232885357hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17844421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241308
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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