A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6191n54



Internal ID18998367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137402..1138048hg38UCSC Ensembl
chr19:1137401..1138047hg19UCSC Ensembl
chr19:1088401..1089047hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38647
hg19647
hg18647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578235, nsv578234
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6191n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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