A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892095



Internal ID19186491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103591783..103755481hg38UCSC Ensembl
Outerchr11:103591783..103755481hg38UCSC Ensembl
Innerchr11:103462511..103626209hg19UCSC Ensembl
Outerchr11:103462511..103626209hg19UCSC Ensembl
Innerchr11:102967721..103131419hg18UCSC Ensembl
Outerchr11:102967721..103131419hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38163699
hg19163699
hg18163699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780005, essv25782785, essv25779934
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892095
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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