A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160029



Internal ID21488509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117843400..117843400hg38UCSC Ensembl
chr9:120605678..120605678hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637570
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160029
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