A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837453



Internal ID22612388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91444398..91451770hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496843, nssv17496844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837453
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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