A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778563



Internal ID18826697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28209080..28291550hg38UCSC Ensembl
Innerchr11:28230627..28313097hg19UCSC Ensembl
Innerchr11:28187203..28269673hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3882471
hg1982471
hg1882471
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891961
Supporting Variants
Samples
Known GenesMETTL15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778563
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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