A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427347



Internal ID21084900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124370801..124373400hg38UCSC Ensembl
chr8:125383042..125385641hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236450
Samples
Known GenesTMEM65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427347
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer