A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587435



Internal ID21535995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19145057..19209866hg38UCSC Ensembl
chr9:19145055..19209864hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3864810
hg1964810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161394
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587435
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