A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139666



Internal ID21486654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:445896..446000hg38UCSC Ensembl
chr8:395896..396000hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578571
Supporting Variants
SamplesNA12878
Known GenesFBXO25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139666
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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