A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090867



Internal ID21401665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829649..89831981hg38UCSC Ensembl
chr16:89896057..89898389hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588392
Supporting Variants
SamplesHG00096
Known GenesSPIRE2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090867
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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