A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142681



Internal ID21420098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109149979..109149979hg38UCSC Ensembl
chr9:111912259..111912259hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626784
Supporting Variants
SamplesHG00731
Known GenesFRRS1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142681
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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