A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874662



Internal ID22649616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50670867..50674096hg38UCSC Ensembl
chr22:51109295..51112524hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg383230
hg193230
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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