A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797338



Internal ID18831850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20540113..20628616hg38UCSC Ensembl
Innerchr11:20561659..20650162hg19UCSC Ensembl
Innerchr11:20518235..20606738hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3888504
hg1988504
hg1888504
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891940
Supporting Variants
Samples
Known GenesSLC6A5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=41
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797338
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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