A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024695



Internal ID21934038
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 StatusM
Merged Variants
Supporting Variantsnssv17597587
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024695
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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