A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943393



Internal ID22718842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20038752..20231884hg38UCSC Ensembl
chr14:20506911..20700043hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38193133
hg19193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379563
Samples
Known GenesOR11G2, OR11H6, OR4K17, OR4L1, OR4N5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943393
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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