A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013499



Internal ID21922842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94797069..94847072hg38UCSC Ensembl
chr10:96556826..96606829hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3850004
hg1950004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590158
Samples
Known GenesCYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013499
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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