A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247426



Internal ID22052036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99719841..99719841hg38UCSC Ensembl
chr10:101479598..101479598hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841975
Samples
Known GenesCOX15
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247426
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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