A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597587



Internal ID21789630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79598997..79608834hg38UCSC Ensembl
chr14:80065340..80075177hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg389838
hg199838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024695
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597587
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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