A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6186n54



Internal ID18998362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1130987..1138268hg38UCSC Ensembl
chr19:1130986..1138267hg19UCSC Ensembl
chr19:1081986..1089267hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387282
hg197282
hg187282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578220, nsv578219, nsv578218
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6186n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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