A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600858



Internal ID21549501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75904301..75904491hg38UCSC Ensembl
chr15:76196642..76196832hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089185
SamplesHG02818
Known GenesFBXO22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600858
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