A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739869



Internal ID20515845
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 StatusM
Merged Variants
Supporting Variantsnssv16285090
Samples
Known GenesCARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739869
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