A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063836



Internal ID21973069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99771163..99771163hg38UCSC Ensembl
chr7:99368786..99368786hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574794
Samples
Known GenesCYP3A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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