A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890408



Internal ID22665435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147402341..147402652hg38UCSC Ensembl
chr5:146781904..146782215hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409959
Samples
Known GenesDPYSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890408
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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