A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049405



Internal ID21958638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591593..31591645hg38UCSC Ensembl
chr22:31987579..31987631hg19UCSC 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 Variantsnssv17638653
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049405
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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