A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046747



Internal ID21955980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31514287..31514339hg38UCSC Ensembl
chr22:31910273..31910325hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646642
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046747
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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