A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613209



Internal ID21805256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102888135..102888135hg38UCSC Ensembl
chr14:103354472..103354472hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088231
Supporting Variants
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613209
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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