A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789902



Internal ID19163123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97426218..97760874hg38UCSC Ensembl
Innerchr11:97297218..97631874hg19UCSC Ensembl
Innerchr11:96802428..97137084hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38334657
hg19334657
hg18334657
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892080
Supporting Variants
Samples
Known GenesMIR7976
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=72
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789902
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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