A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596189



Internal ID21544796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60516173..60516236hg38UCSC Ensembl
chr15:60808372..60808435hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091856
SamplesHG00732
Known GenesRORA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596189
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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