A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247228



Internal ID22051838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70243859..70243859hg38UCSC Ensembl
chr10:72003615..72003615hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247228
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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