A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761815



Internal ID20537675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22765817..22765817hg38UCSC Ensembl
chr8:22623330..22623330hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262380
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761815
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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