A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836130



Internal ID22611065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24951681..24967914hg38UCSC Ensembl
chr3:24993172..25009405hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3816234
hg1916234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836130
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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