A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240457



Internal ID22045067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22413088..22413088hg38UCSC Ensembl
chr10:22702017..22702017hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842033
Samples
Known GenesSPAG6
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240457
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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