A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631088



Internal ID21579393
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 StatusM
Merged Variants
Supporting Variantsnssv17163079
SamplesHG00513
Known GenesNTRK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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