A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892080



Internal ID19186476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97469385..97760874hg38UCSC Ensembl
Outerchr11:97426218..97760874hg38UCSC Ensembl
Innerchr11:97340385..97631874hg19UCSC Ensembl
Outerchr11:97297218..97631874hg19UCSC Ensembl
Innerchr11:96845595..97137084hg18UCSC Ensembl
Outerchr11:96802428..97137084hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38334657
hg19334657
hg18334657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789902, essv25789361, essv25790235
Samples
Known GenesMIR7976
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892080
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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