A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945409



Internal ID22720886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79604510..79605764hg38UCSC Ensembl
chr14:80070853..80072107hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371872
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945409
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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