A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522166



Internal ID298439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68598529..68604966hg38UCSC Ensembl
chr15:68890868..68897305hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386438
hg196438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703907
Samples
Known GenesCORO2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522166
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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