A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424718



Internal ID21082271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139704201..140110200hg38UCSC Ensembl
chr8:140716444..141120299hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38406000
hg19403856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7524n223
Supporting Variantsnssv18233905
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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