A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240458



Internal ID22045068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22433856..22433856hg38UCSC Ensembl
chr10:22722785..22722785hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240458
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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