A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251400



Internal ID22056010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34220971..34220971hg38UCSC Ensembl
chr20:32808777..32808777hg19UCSC Ensembl
Cytoband20q11.22
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 Variantsnssv17849948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251400
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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