A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6199n54



Internal ID18998375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1460474..1470585hg38UCSC Ensembl
chr19:1460473..1470584hg19UCSC Ensembl
chr19:1411473..1421584hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810112
hg1910112
hg1810112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578284, nsv578282, nsv578281
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6199n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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