A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838821



Internal ID22613756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186076599..186113014hg38UCSC Ensembl
chr4:186997753..187034168hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3836416
hg1936416
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493703
Samples
Known GenesTLR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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