A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568290



Internal ID21516636
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 Variantsnssv17159135
SamplesHG00732
Known GenesCYP3A43
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568290
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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