A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753738



Internal ID20529598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17369342..17369342hg38UCSC Ensembl
chr22:17850241..17850241hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753738
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer