A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532069



Internal ID308000
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 StatusM
Merged Variants
Supporting Variantsnssv17703669
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532069
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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