A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002913



Internal ID69556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99648654..99657137hg38UCSC Ensembl
chr7:99246277..99254760hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388484
hg198484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474863
Supporting Variants
Samples
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002913
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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