A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744465



Internal ID20520464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46248999..46249053hg38UCSC Ensembl
chr22:46644896..46644950hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295035
Samples
Known GenesCDPF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744465
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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