A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220137



Internal ID22364929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18237694..18242476hg38UCSC Ensembl
chr19:18348504..18353286hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384783
hg194783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286965, nssv14286966
SamplesNA19238, NA19239
Known GenesPDE4C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220137
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer