A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891940



Internal ID18839650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20540113..20628616hg38UCSC Ensembl
Outerchr11:20540113..20628616hg38UCSC Ensembl
Innerchr11:20561659..20650162hg19UCSC Ensembl
Outerchr11:20561659..20650162hg19UCSC Ensembl
Innerchr11:20518235..20606738hg18UCSC Ensembl
Outerchr11:20518235..20606738hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3888504
hg1988504
hg1888504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797338
Samples
Known GenesSLC6A5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891940
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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