A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931392



Internal ID22706675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102812701..102812827hg38UCSC Ensembl
chr14:103279038..103279164hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374601
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931392
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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