A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529520



Internal ID22398912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39291894..39292501hg38UCSC Ensembl
chr17:37448147..37448754hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387903, nssv14383982
SamplesNA19238, NA19240
Known GenesFBXL20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529520
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