A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902116



Internal ID22677270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107783956..107784026hg38UCSC Ensembl
chr5:107119657..107119727hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902116
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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