A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866106



Internal ID22641041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68818839..68820071hg38UCSC Ensembl
chr11:68586307..68587539hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458749
Samples
Known GenesCPT1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866106
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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