A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942745



Internal ID22718187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55320695..55320917hg38UCSC Ensembl
chr19:55832063..55832285hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391615
Samples
Known GenesTMEM150B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942745
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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