A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908776



Internal ID22683986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86517373..86518089hg38UCSC Ensembl
chr9:89132288..89133004hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908776
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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