A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362279



Internal ID21019832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133050189..133050705hg38UCSC Ensembl
chr3:132769033..132769549hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094209
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362279
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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