A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037903



Internal ID21947246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79604510..79605765hg38UCSC Ensembl
chr14:80070853..80072108hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603591
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer