A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051206



Internal ID21960439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19084669..19084723hg38UCSC Ensembl
chr22:19072182..19072236hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637739
Samples
Known GenesDGCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051206
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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