A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903394



Internal ID22678561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55612766..55615212hg38UCSC Ensembl
chr5:54908594..54911040hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382447
hg192447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903394
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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