A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452430



Internal ID21109983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94670157..94794660hg38UCSC Ensembl
chr10:96429914..96554417hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38124504
hg19124504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv857n223
Supporting Variantsnssv17985286
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452430
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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