A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160134



Internal ID21479453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132526542..132529522hg38UCSC Ensembl
chr9:135401929..135404909hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594674
Supporting Variants
SamplesHG03486
Known GenesC9orf171
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160134
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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