A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587677



Internal ID21536235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451376..93451448hg38UCSC Ensembl
chr9:96213658..96213730hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163272
SamplesHG02818
Known GenesFAM120AOS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587677
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