A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921333



Internal ID22696556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89483670..89483733hg38UCSC Ensembl
chr9:92098585..92098648hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921333
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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