A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920668



Internal ID22695891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89724788..89728691hg38UCSC Ensembl
chr8:90737016..90740919hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383904
hg193904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920668
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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