A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578742



Internal ID16019465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18057864..18070969hg38UCSC Ensembl
Innerchr19:18168674..18181779hg19UCSC Ensembl
Innerchr19:18029674..18042779hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3813106
hg1913106
hg1813106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895733
Samples
Known GenesIL12RB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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