A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560420



Internal ID22429216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76231963..76231963hg38UCSC Ensembl
chr14:76698306..76698306hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14371981, nssv14371982, nssv14371983
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560420
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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