A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969110



Internal ID22744045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28768260..28768260hg38UCSC Ensembl
chr22:29164248..29164248hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969110
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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