A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036538



Internal ID92103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94812402..94829156hg38UCSC Ensembl
chr10:96572159..96588913hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3816755
hg1916755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490742
Supporting Variants
Samples
Known GenesCYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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