A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589251



Internal ID21537815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86842993..86843357hg38UCSC Ensembl
chr9:89457908..89458272hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162935
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589251
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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