A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764308



Internal ID20540168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86024254..86024254hg38UCSC Ensembl
chr16:86057860..86057860hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764308
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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