A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560720



Internal ID22429517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68286870..68286870hg38UCSC Ensembl
chr15:68579208..68579208hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385623
SamplesNA19238
Known GenesFEM1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560720
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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