A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925899



Internal ID22701126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22750057..22750350hg38UCSC Ensembl
chr8:22607570..22607863hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434044
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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