A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251317



Internal ID22055927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21598764..21598764hg38UCSC Ensembl
chr20:21579402..21579402hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251317
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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