A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516926



Internal ID293366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92402408..92407467hg38UCSC Ensembl
chr15:92945638..92950697hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385060
hg195060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703685
Samples
Known GenesST8SIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516926
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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