A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918450



Internal ID22693671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24072394..24079670hg38UCSC Ensembl
chr8:23929907..23937183hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg387277
hg197277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918450
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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