A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917935



Internal ID22693156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19729751..19733534hg38UCSC Ensembl
chr8:19587262..19591045hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917935
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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