A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589155



Internal ID21537719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44210387..44210442hg38UCSC Ensembl
chr22:44606267..44606322hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122067
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589155
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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