A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898196



Internal ID22673309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175319429..175324112hg38UCSC Ensembl
chr5:174746432..174751115hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg384684
hg194684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898196
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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