A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223808



Internal ID20790848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24761112..24778561hg38UCSC Ensembl
chr9:24761110..24778559hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3817450
hg1917450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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