A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032999



Internal ID21942342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102819964..102857203hg38UCSC Ensembl
chr14:103286301..103323540hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3837240
hg1937240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609107
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032999
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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