A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285090



Internal ID20494308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37491556..37491879hg38UCSC Ensembl
chr22:37887594..37887886hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38324
hg19293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739869
Supporting Variants
Samples
Known GenesCARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285090
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