A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163079



Internal ID21412279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84797660..84797660hg38UCSC Ensembl
chr9:87412575..87412575hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631088
Supporting Variants
SamplesHG00513
Known GenesNTRK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163079
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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