A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790981



Internal ID19163226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83847695..83875794hg38UCSC Ensembl
Innerchr11:83558738..83586837hg19UCSC Ensembl
Innerchr11:83236386..83264485hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3828100
hg1928100
hg1828100
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892040
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790981
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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