A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760085



Internal ID20535945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99675595..99675595hg38UCSC Ensembl
chr7:99273218..99273218hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275492
Samples
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760085
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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