A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076418



Internal ID21479798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92705312..92705312hg38UCSC Ensembl
chr11:92438478..92438478hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650659
Supporting Variants
SamplesHG03486
Known GenesFAT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076418
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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