A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595732



Internal ID21544339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79001248..79001326hg38UCSC Ensembl
chr15:79293590..79293668hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083381
SamplesHG03486
Known GenesRASGRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595732
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