A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159978



Internal ID21401471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133391278..133391278hg38UCSC Ensembl
chr9:136257054..136257054hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641803
Supporting Variants
SamplesHG00096
Known GenesC9orf96
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159978
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