A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432884



Internal ID22490754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84593321..84593450hg38UCSC Ensembl
chr9:87208236..87208365hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432884
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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