A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240392



Internal ID22045002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12133790..12133790hg38UCSC Ensembl
chr10:12175789..12175789hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841822
Samples
Known GenesSEC61A2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240392
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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