A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933665



Internal ID22708979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11425183..11425312hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933665
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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