A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579285



Internal ID16366694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30788677..30798281hg38UCSC Ensembl
Innerchr19:31279584..31289188hg19UCSC Ensembl
Innerchr19:35971424..35981028hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg389605
hg199605
hg189605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897587
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579285
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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