A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232472



Internal ID20799512
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 StatusS
Merged Variantsnsv6427568
Supporting Variants
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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