A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892083



Internal ID19186479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97730350..97779416hg38UCSC Ensembl
Outerchr11:97709596..97779416hg38UCSC Ensembl
Innerchr11:97601350..97650416hg19UCSC Ensembl
Outerchr11:97580596..97650416hg19UCSC Ensembl
Innerchr11:97106560..97155626hg18UCSC Ensembl
Outerchr11:97085806..97155626hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3869821
hg1969821
hg1869821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783956, essv25778875
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892083
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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