A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563114



Internal ID22431854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3790607..3790607hg38UCSC Ensembl
chr3:3832291..3832291hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303753, nssv14303752
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563114
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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