A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891960



Internal ID19186356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28176014..28209080hg38UCSC Ensembl
Outerchr11:28176014..28209080hg38UCSC Ensembl
Innerchr11:28197561..28230627hg19UCSC Ensembl
Outerchr11:28197561..28230627hg19UCSC Ensembl
Innerchr11:28154137..28187203hg18UCSC Ensembl
Outerchr11:28154137..28187203hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3833067
hg1933067
hg1833067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786148
Samples
Known GenesMETTL15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891960
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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