A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640416



Internal ID21588721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95139851..95139851hg38UCSC Ensembl
chr9:97902133..97902133hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163771
SamplesHG02818
Known GenesFANCC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640416
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer