A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922089



Internal ID22697314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23290081..23299890hg38UCSC Ensembl
chr9:23290079..23299888hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389810
hg199810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922089
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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