A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240481



Internal ID22045091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24650449..24650449hg38UCSC Ensembl
chr10:24939378..24939378hg19UCSC Ensembl
Cytoband10p12.1
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 Variantsnssv17842057
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240481
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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