A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911233



Internal ID22686446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99863766..99865938hg38UCSC Ensembl
chr7:99461389..99463561hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382173
hg192173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448709
Samples
Known GenesCYP3A43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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