A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097439



Internal ID21484918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102877254..102877254hg38UCSC Ensembl
chr14:103343591..103343591hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646856
Supporting Variants
SamplesNA12329
Known GenesTRAF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097439
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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