A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840980



Internal ID22615915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109688101..109691410hg38UCSC Ensembl
chr5:109023802..109027111hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg383310
hg193310
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493023
Samples
Known GenesMAN2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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