A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766657



Internal ID20542517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153163764..153163764hg38UCSC Ensembl
chr4:154084916..154084916hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284394
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766657
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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