A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017408



Internal ID21926751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656475..24657348hg38UCSC Ensembl
chr10:24945404..24946277hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594852
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017408
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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