A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891958



Internal ID18839668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28066977..28124180hg38UCSC Ensembl
Outerchr11:28066977..28124180hg38UCSC Ensembl
Innerchr11:28088524..28145727hg19UCSC Ensembl
Outerchr11:28088524..28145727hg19UCSC Ensembl
Innerchr11:28045100..28102303hg18UCSC Ensembl
Outerchr11:28045100..28102303hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3857204
hg1957204
hg1857204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789939
Samples
Known GenesKIF18A, METTL15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891958
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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