A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162627



Internal ID21485438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72647782..72647782hg38UCSC Ensembl
chr9:75262698..75262698hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382284
hg192284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639806
Supporting Variants
SamplesNA12878
Known GenesTMC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162627
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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