A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492381



Internal ID269595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94930837..95095277hg38UCSC Ensembl
chr10:96690594..96855034hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38164441
hg19164441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036557
Samples
Known GenesCYP2C8, CYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492381
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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