A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782660



Internal ID18833889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14839971..14950061hg38UCSC Ensembl
Innerchr11:14861517..14971607hg19UCSC Ensembl
Innerchr11:14818093..14928183hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38110091
hg19110091
hg18110091
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891931
Supporting Variants
Samples
Known GenesCYP2R1, PDE3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782660
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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