A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225453



Internal ID22368575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293090..91293480hg38UCSC Ensembl
chr14:91759434..91759824hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384672
SamplesNA19240
Known GenesCCDC88C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225453
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