A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749710



Internal ID20525743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78879952..78880265hg38UCSC Ensembl
chr14:79346295..79346608hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281491
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749710
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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