A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6187n54



Internal ID18998363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1136224..1154384hg38UCSC Ensembl
chr19:1136223..1154383hg19UCSC Ensembl
chr19:1087223..1105383hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818161
hg1918161
hg1818161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578232, nsv578267, nsv578265, nsv578258, nsv578233, nsv578224, nsv578251, nsv578240
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6187n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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