A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390550



Internal ID21381685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81858342..81858661hg38UCSC Ensembl
chr3:81907493..81907812hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707147
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390550
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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