A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563139



Internal ID22431879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79619066..79619066hg38UCSC Ensembl
chr3:79668216..79668216hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307043
SamplesNA19239
Known GenesROBO1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563139
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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