A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859793



Internal ID22634728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69598498..69615621hg38UCSC Ensembl
chr11:69413266..69430389hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3817124
hg1917124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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