A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110402



Internal ID18920648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42125795..42137591hg38UCSC Ensembl
Outerchr22:42521800..42533600hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811797
hg1911801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960053
SamplesKWS1
Known GenesCYP2D6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110402
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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