A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593350



Internal ID21541936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238007..98238825hg38UCSC Ensembl
chr9:101000289..101001107hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163433
SamplesNA19238
Known GenesTBC1D2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593350
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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