A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765205



Internal ID20541065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49775819..49775819hg38UCSC Ensembl
chr22:50169467..50169467hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273717
Samples
Known GenesBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765205
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