A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857378



Internal ID22632313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89695423..89712955hg38UCSC Ensembl
chr11:89428591..89446123hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3817533
hg1917533
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458238, nssv17462758
Samples
Known GenesFOLH1B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857378
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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