A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880526



Internal ID22655496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37881259..37882658hg38UCSC Ensembl
chr22:38277266..38278665hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482939
Samples
Known GenesEIF3L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880526
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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