A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891931



Internal ID18839641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14839971..14950061hg38UCSC Ensembl
Outerchr11:14839971..14950061hg38UCSC Ensembl
Innerchr11:14861517..14971607hg19UCSC Ensembl
Outerchr11:14861517..14971607hg19UCSC Ensembl
Innerchr11:14818093..14928183hg18UCSC Ensembl
Outerchr11:14818093..14928183hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38110091
hg19110091
hg18110091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782660
Samples
Known GenesCYP2R1, PDE3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891931
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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