A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604080



Internal ID21552747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98024274..98027013hg38UCSC Ensembl
chr9:100786556..100789295hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163427
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604080
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