A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899389



Internal ID16193345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40843827..40878673hg38UCSC Ensembl
Innerchr19:41349732..41384578hg19UCSC Ensembl
Innerchr19:46041572..46076418hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3834847
hg1934847
hg1834847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579526
Supporting Variants
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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