A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841425



Internal ID22616360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134345016..134354676hg38UCSC Ensembl
chr5:133680707..133690367hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg389661
hg199661
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495492
Samples
Known GenesCDKL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841425
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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