A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911706



Internal ID22686921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43219425..43220487hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911706
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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