A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433256



Internal ID21395258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24377365..24379364hg38UCSC Ensembl
chr20:24358001..24360000hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749281
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433256
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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