A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786148



Internal ID19163497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28176014..28209080hg38UCSC Ensembl
Innerchr11:28197561..28230627hg19UCSC Ensembl
Innerchr11:28154137..28187203hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3833067
hg1933067
hg1833067
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891960
Supporting Variants
Samples
Known GenesMETTL15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786148
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