A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892108



Internal ID19186504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129823771..129850005hg38UCSC Ensembl
Outerchr11:129823771..129850005hg38UCSC Ensembl
Innerchr11:129693666..129719900hg19UCSC Ensembl
Outerchr11:129693666..129719900hg19UCSC Ensembl
Innerchr11:129198876..129225110hg18UCSC Ensembl
Outerchr11:129198876..129225110hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3826235
hg1926235
hg1826235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798428
Samples
Known GenesTMEM45B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892108
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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