A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600679



Internal ID21549320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18175853..18176168hg38UCSC Ensembl
chr22:18658620..18658935hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123975
SamplesHG00514
Known GenesUSP18
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600679
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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