A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879052



Internal ID22654019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28084666..28088543hg38UCSC Ensembl
chr22:28480654..28484531hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383878
hg193878
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482823
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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