A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162905



Internal ID21466346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86052766..86052766hg38UCSC Ensembl
chr9:88667681..88667681hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631811
Supporting Variants
SamplesHG03065
Known GenesGOLM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162905
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