A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046939



Internal ID21956173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20567643..20567708hg38UCSC Ensembl
chr22:20921930..20921995hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647576
Samples
Known GenesMED15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046939
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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