A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760609



Internal ID20536469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140349241..140349241hg38UCSC Ensembl
chr8:141359340..141359340hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281727
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760609
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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