A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560463



Internal ID22429260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57480248..57480248hg38UCSC Ensembl
chr15:57772446..57772446hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381888, nssv14381709, nssv14387998
SamplesNA19239, HG00731, HG00733
Known GenesCGNL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560463
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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