A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079943



Internal ID21989176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99771312..99771312hg38UCSC Ensembl
chr7:99368935..99368935hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571463
Samples
Known GenesCYP3A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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