A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067035



Internal ID21486633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84368292..84368292hg38UCSC Ensembl
chr1:84833975..84833975hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609641
Supporting Variants
SamplesNA12878
Known GenesUOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067035
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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