A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899462



Internal ID16193418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850414..40873243hg38UCSC Ensembl
Innerchr19:41356319..41379148hg19UCSC Ensembl
Innerchr19:46048159..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822830
hg1922830
hg1822830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579562
Supporting Variants
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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