A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929638



Internal ID22704894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21494333..21494474hg38UCSC Ensembl
chr14:21962492..21962633hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374326
Samples
Known GenesTOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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