A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089514



Internal ID21998747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24710937..24710937hg38UCSC Ensembl
chr10:24999866..24999866hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597273
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089514
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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