A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6194n54



Internal ID18998370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137713..1148867hg38UCSC Ensembl
chr19:1137712..1148866hg19UCSC Ensembl
chr19:1088712..1099866hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811155
hg1911155
hg1811155
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578260, nsv578257
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6194n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss4
Observed Complex0
Frequencyn/a


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