A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847825



Internal ID22622760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89616581..89617906hg38UCSC Ensembl
chr14:90082925..90084250hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv611n209
Supporting Variantsnssv17469737
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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