A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856411



Internal ID22631346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91941091..91946295hg38UCSC Ensembl
chr14:92407435..92412639hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385205
hg195205
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469756
Samples
Known GenesFBLN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856411
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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