A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703660



Internal ID127326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92025742..92028444hg38UCSC Ensembl
chr15:92568972..92571674hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522874
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703660
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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