A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226146



Internal ID20793186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32080901..32088800hg38UCSC Ensembl
chr9:32080899..32088798hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00093


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