A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836298



Internal ID22611233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47282139..47283338hg38UCSC Ensembl
chr3:47323629..47324828hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492536, nssv17492535
Samples
Known GenesKIF9, KLHL18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836298
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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