A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074778



Internal ID21984011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22728586..22728586hg38UCSC Ensembl
chr8:22586099..22586099hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574416
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074778
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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