A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227745



Internal ID22370143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101555387..101557443hg38UCSC Ensembl
chr14:102021724..102023780hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382057
hg192057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385766
SamplesHG00512
Known GenesDIO3OS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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