A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761208



Internal ID20537068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153068928..153068928hg38UCSC Ensembl
chr5:152448488..152448488hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761208
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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