A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033530



Internal ID21942873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78822993..78837897hg38UCSC Ensembl
chr14:79289336..79304240hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3814905
hg1914905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612573
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033530
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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