A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865211



Internal ID22640146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134012485..134014584hg38UCSC Ensembl
chr11:133882380..133884479hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865211
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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