A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836835



Internal ID22611770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81211390..81223707hg38UCSC Ensembl
chr3:81260541..81272858hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3812318
hg1912318
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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