A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565461



Internal ID22434180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30786497..30786497hg38UCSC Ensembl
chr8:30644013..30644013hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340414, nssv14340415
SamplesNA19238, NA19240
Known GenesPPP2CB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565461
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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