A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899405



Internal ID16193361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40848628..40875598hg38UCSC Ensembl
Innerchr19:41354533..41381503hg19UCSC Ensembl
Innerchr19:46046373..46073343hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3826971
hg1926971
hg1826971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579539
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)nssv899405
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