A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6189n54



Internal ID18998365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137305..1138268hg38UCSC Ensembl
chr19:1137304..1138267hg19UCSC Ensembl
chr19:1088304..1089267hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578229, nsv578246, nsv578230, nsv578237
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6189n54
Frequency
Sample Size17421
Observed Gain67
Observed Loss21
Observed Complex0
Frequencyn/a


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