A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859455



Internal ID22634390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55589430..55599982hg38UCSC Ensembl
chr10:57349190..57359742hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3810553
hg1910553
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464108
Samples
Known GenesMTRNR2L5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859455
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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