A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792301



Internal ID18819119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67768190..67947557hg38UCSC Ensembl
Innerchr11:67535661..67715028hg19UCSC Ensembl
Innerchr11:67292237..67471604hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38179368
hg19179368
hg18179368
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892023
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792301
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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