A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782160



Internal ID18812963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55639307hg38UCSC Ensembl
Innerchr11:55373973..55406783hg19UCSC Ensembl
Innerchr11:55130549..55163359hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3832811
hg1932811
hg1832811
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892007
Supporting Variants
Samples
Known GenesOR4P4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782160
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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