A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407330



Internal ID186664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94986140..94986191hg38UCSC Ensembl
chr10:96745897..96745948hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036563
Samples
Known GenesCYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407330
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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