A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854581



Internal ID22629516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68816592..68826598hg38UCSC Ensembl
chr11:68584060..68594066hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810007
hg1910007
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463543
Samples
Known GenesCPT1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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