A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748408



Internal ID20524433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27770667..27770732hg38UCSC Ensembl
chr22:28166655..28166720hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294352
Samples
Known GenesMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748408
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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