A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785117



Internal ID18829256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90256319..90830753hg38UCSC Ensembl
Innerchr11:89989487..90563921hg19UCSC Ensembl
Innerchr11:89629135..90203569hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38574435
hg19574435
hg18574435
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892063
Supporting Variants
Samples
Known GenesDISC1FP1, MIR4490
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=126
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785117
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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