A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010278



Internal ID74484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22728512..22728592hg38UCSC Ensembl
chr8:22586025..22586105hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492190
Supporting Variants
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010278
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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