A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423859



Internal ID21081412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28441946..28449322hg38UCSC Ensembl
chr8:28299463..28306839hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg387377
hg197377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236627
Samples
Known GenesFBXO16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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