A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836284



Internal ID22611219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45979842..45981291hg38UCSC Ensembl
chr3:46021334..46022783hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491549
Samples
Known GenesFYCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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