A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546862



Internal ID320768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20041000..20075564hg38UCSC Ensembl
chr22:20028523..20063087hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3834565
hg1934565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727676
Samples
Known GenesTANGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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