A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063404



Internal ID21972637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140349411..140349411hg38UCSC Ensembl
chr8:141359510..141359510hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589644
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063404
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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