A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448831



Internal ID21106384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94678827..94872441hg38UCSC Ensembl
chr10:96438584..96632198hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38193615
hg19193615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985288
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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