A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418793



Internal ID21076346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139925930..140083904hg38UCSC Ensembl
chr8:140938174..141094003hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38157975
hg19155830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167211
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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