A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450810



Internal ID21108363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80298743..80463153hg38UCSC Ensembl
chr9:82913658..83078068hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38164411
hg19164411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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