A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474782



Internal ID252433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99846640..99847124hg38UCSC Ensembl
chr7:99444263..99444747hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002920
Samples
Known GenesCYP3A43
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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