A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917894



Internal ID22693115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94765833..94939358hg38UCSC Ensembl
chr10:96525590..96699115hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38173526
hg19173526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351454
Samples
Known GenesCYP2C19, CYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917894
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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