A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745056



Internal ID20521061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36091472..36091591hg38UCSC Ensembl
chr22:36487520..36487639hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745056
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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