A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758166



Internal ID20534026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124309864..124309864hg38UCSC Ensembl
chr8:125322105..125322105hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758166
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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