A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051147



Internal ID21960380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45501115..45501183hg38UCSC Ensembl
chr22:45896995..45897063hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051147
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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