A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126117



Internal ID21486618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14041655..14041655hg38UCSC Ensembl
chr3:14083155..14083155hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614483
Supporting Variants
SamplesNA12878
Known GenesTPRXL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126117
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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