A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862413



Internal ID22637348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108099123..108109259hg38UCSC Ensembl
chr11:107969850..107979986hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810137
hg1910137
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458578
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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