A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698411



Internal ID122077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102877002..102877362hg38UCSC Ensembl
chr14:103343339..103343699hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497158
Supporting Variants
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698411
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.029825


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