A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642797



Internal ID21591102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114926982..114926982hg38UCSC Ensembl
chr9:117689262..117689262hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160241
SamplesHG00171
Known GenesTNFSF8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642797
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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