A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225446



Internal ID22368569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14852091..14903313hg38UCSC Ensembl
chr19:14962903..15014125hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851223
hg1951223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286150, nssv14286151
SamplesHG00731, HG00732
Known GenesOR7A17
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225446
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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