A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785722



Internal ID19175726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84954725..84997738hg38UCSC Ensembl
Innerchr11:84665769..84708782hg19UCSC Ensembl
Innerchr11:84343417..84386430hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843014
hg1943014
hg1843014
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892045
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785722
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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