A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427568



Internal ID21085121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22901931..22919597hg38UCSC Ensembl
chr8:22759444..22777110hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3817667
hg1917667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232472
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427568
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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