A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6188n54



Internal ID18998364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137305..1138161hg38UCSC Ensembl
chr19:1137304..1138160hg19UCSC Ensembl
chr19:1088304..1089160hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38857
hg19857
hg18857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578226, nsv578228, nsv578227, nsv578225
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6188n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer