A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568133



Internal ID21516477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37506306..37506444hg38UCSC Ensembl
chr8:37363824..37363962hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149962
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568133
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