A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797640



Internal ID18828703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55660224hg38UCSC Ensembl
Innerchr11:55373973..55427700hg19UCSC Ensembl
Innerchr11:55130549..55184276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3853728
hg1953728
hg1853728
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892007
Supporting Variants
Samples
Known GenesOR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797640
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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