A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036561



Internal ID92119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94984164..94984215hg38UCSC Ensembl
chr10:96743921..96743972hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5402421
Supporting Variants
Samples
Known GenesCYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036561
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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