A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862343



Internal ID22637278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89698305..89720424hg38UCSC Ensembl
chr11:89431473..89453592hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3822120
hg1922120
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453876, nssv17464638
Samples
Known GenesFOLH1B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862343
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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