A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892045



Internal ID19186441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84954725..84997738hg38UCSC Ensembl
Outerchr11:84954725..84997738hg38UCSC Ensembl
Innerchr11:84665769..84708782hg19UCSC Ensembl
Outerchr11:84665769..84708782hg19UCSC Ensembl
Innerchr11:84343417..84386430hg18UCSC Ensembl
Outerchr11:84343417..84386430hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843014
hg1943014
hg1843014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785722
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892045
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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