A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434474



Internal ID21092027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140387818..140391649hg38UCSC Ensembl
chr8:141397917..141401748hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383832
hg193832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167242
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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