A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892110



Internal ID18839820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131743728..131788233hg38UCSC Ensembl
Outerchr11:131743728..131788233hg38UCSC Ensembl
Innerchr11:131613622..131658127hg19UCSC Ensembl
Outerchr11:131613622..131658127hg19UCSC Ensembl
Innerchr11:131118832..131163337hg18UCSC Ensembl
Outerchr11:131118832..131163337hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3844506
hg1944506
hg1844506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793024
Samples
Known GenesNTM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892110
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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