A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594569



Internal ID21543168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38241959..38242038hg38UCSC Ensembl
chr9:38241956..38242035hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162183
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594569
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