A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015969



Internal ID21925312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99728161..99728306hg38UCSC Ensembl
chr7:99325784..99325929hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567177
Samples
Known GenesCYP3A7, CYP3A7-CYP3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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