A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892002



Internal ID18839712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49916027..50771311hg38UCSC Ensembl
Outerchr11:49916027..50771311hg38UCSC Ensembl
Innerchr11:49937579..50730482hg19UCSC Ensembl
Outerchr11:49937579..50730482hg19UCSC Ensembl
Innerchr11:49894155..50687058hg18UCSC Ensembl
Outerchr11:49894155..50687058hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38855285
hg19792904
hg18792904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789881
Samples
Known GenesLOC441601, LOC646813, OR4C12, OR4C13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892002
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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