A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560393



Internal ID22429190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101849672..101849672hg38UCSC Ensembl
chr14:102316009..102316009hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388060, nssv14377018
SamplesHG00732, HG00733
Known GenesPPP2R5C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560393
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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