A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891927



Internal ID19186323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7686537..7909093hg38UCSC Ensembl
Outerchr11:7686537..7909093hg38UCSC Ensembl
Innerchr11:7707768..7930640hg19UCSC Ensembl
Outerchr11:7707768..7930640hg19UCSC Ensembl
Innerchr11:7664344..7887216hg18UCSC Ensembl
Outerchr11:7664344..7887216hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38222557
hg19222873
hg18222873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782979
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3, OVCH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891927
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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