A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892027



Internal ID19186423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78539325..78645453hg38UCSC Ensembl
Outerchr11:78539325..78645453hg38UCSC Ensembl
Innerchr11:78250371..78356498hg19UCSC Ensembl
Outerchr11:78250371..78356498hg19UCSC Ensembl
Innerchr11:77928019..78034146hg18UCSC Ensembl
Outerchr11:77928019..78034146hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38106129
hg19106128
hg18106128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792834
Samples
Known GenesNARS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892027
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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