A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703659



Internal ID127325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92016279..92016292hg38UCSC Ensembl
chr15:92559509..92559522hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552993
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010775


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