A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578640



Internal ID16019363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14019403..14042481hg38UCSC Ensembl
Innerchr19:14130215..14153293hg19UCSC Ensembl
Innerchr19:13991215..14014293hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3823079
hg1923079
hg1823079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894810
Samples
Known GenesIL27RA, RLN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578640
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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