A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560680



Internal ID22429476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79462861..79462861hg38UCSC Ensembl
chr14:79929204..79929204hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390296
SamplesNA19240
Known GenesNRXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560680
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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