A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891981



Internal ID19186377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48031124..48064416hg38UCSC Ensembl
Outerchr11:48031124..48064416hg38UCSC Ensembl
Innerchr11:48052676..48085968hg19UCSC Ensembl
Outerchr11:48052676..48085968hg19UCSC Ensembl
Innerchr11:48009252..48042544hg18UCSC Ensembl
Outerchr11:48009252..48042544hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3833293
hg1933293
hg1833293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783720, essv25784581
Samples
Known GenesPTPRJ
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891981
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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