A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891961



Internal ID18839671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28209080..28291550hg38UCSC Ensembl
Outerchr11:28209080..28291550hg38UCSC Ensembl
Innerchr11:28230627..28313097hg19UCSC Ensembl
Outerchr11:28230627..28313097hg19UCSC Ensembl
Innerchr11:28187203..28269673hg18UCSC Ensembl
Outerchr11:28187203..28269673hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3882471
hg1982471
hg1882471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778563
Samples
Known GenesMETTL15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891961
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