A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260386



Internal ID20469604
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 StatusS
Merged Variantsnsv4758166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260386
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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