A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094209



Internal ID20661249
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 StatusS
Merged Variantsnsv6362279
Supporting Variants
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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