A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740907



Internal ID14738100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15673766..15931354hg38UCSC Ensembl
Innerchr19:15673816..15931304hg38UCSC Ensembl
Outerchr19:15673716..15931404hg38UCSC Ensembl
chr19:15784576..16042164hg19UCSC Ensembl
Innerchr19:15784626..16042114hg19UCSC Ensembl
Outerchr19:15784526..16042214hg19UCSC Ensembl
chr19:15645576..15903164hg18UCSC Ensembl
Innerchr19:15645626..15903114hg18UCSC Ensembl
Outerchr19:15645526..15903214hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38257589
hg19257589
hg18257589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3334671
Supporting Variants
SamplesNA19240
Known GenesCYP4F11, CYP4F12, CYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740907
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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