A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918406



Internal ID22693627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39566056..39900097hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38334042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918406
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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