A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276866



Internal ID20486084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102813159..102813213hg38UCSC Ensembl
chr14:103279496..103279550hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731881
Supporting Variants
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276866
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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