A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589426



Internal ID21537990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16320341..16320433hg38UCSC Ensembl
chr9:16320339..16320431hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161189
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589426
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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