A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853463



Internal ID22628398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43117898..43119482hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381585
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2122n209
Supporting Variantsnssv17513595, nssv17513596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853463
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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