A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891914



Internal ID18839624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4668512..4961931hg38UCSC Ensembl
Outerchr11:4642313..4974456hg38UCSC Ensembl
Innerchr11:4689742..4983161hg19UCSC Ensembl
Outerchr11:4663543..4995686hg19UCSC Ensembl
Innerchr11:4646318..4939737hg18UCSC Ensembl
Outerchr11:4620119..4952262hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38332144
hg19332144
hg18332144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792270, essv25790823
Samples
Known GenesOR51A2, OR51A4, OR51A7, OR51E1, OR51E2, OR51F1, OR51F2, OR51G1, OR51G2, OR51S1, OR51T1, OR52R1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891914
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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