A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801384



Internal ID19162985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98521880..98738663hg38UCSC Ensembl
Innerchr11:98392610..98609393hg19UCSC Ensembl
Innerchr11:97897820..98114603hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38216784
hg19216784
hg18216784
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892086
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=56
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801384
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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