A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895578



Internal ID15842848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15673357..15719658hg38UCSC Ensembl
Innerchr19:15784167..15830468hg19UCSC Ensembl
Innerchr19:15645167..15691468hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3846302
hg1946302
hg1846302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578729
Supporting Variants
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895578
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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