A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600189



Internal ID21548827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102998901..102999046hg38UCSC Ensembl
chr14:103465238..103465383hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092885
SamplesHG02818
Known GenesCDC42BPB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600189
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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