A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703669



Internal ID127335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92146867..92147088hg38UCSC Ensembl
chr15:92690097..92690318hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532069
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004527


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