A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666447



Internal ID21614752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49917986..49917986hg38UCSC Ensembl
chr22:50311634..50311634hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132122
SamplesHG00732
Known GenesALG12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666447
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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