A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854780



Internal ID22629715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85551019..85552273hg38UCSC Ensembl
chr14:86017363..86018617hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469678
Samples
Known GenesFLRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854780
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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