A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563359



Internal ID22432096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9725640..9725640hg38UCSC Ensembl
chr3:9767324..9767324hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304601
SamplesNA19240
Known GenesCPNE9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563359
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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