A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578940



Internal ID16019663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20673648..20804744hg38UCSC Ensembl
Innerchr19:20856454..20987550hg19UCSC Ensembl
Innerchr19:20648294..20779390hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38131097
hg19131097
hg18131097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv1150132
Samples1782681317_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578940
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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