A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891920



Internal ID18839630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5614809..5634163hg38UCSC Ensembl
Outerchr11:5614809..5634163hg38UCSC Ensembl
Innerchr11:5636039..5655393hg19UCSC Ensembl
Outerchr11:5636039..5655393hg19UCSC Ensembl
Innerchr11:5592615..5611969hg18UCSC Ensembl
Outerchr11:5592615..5611969hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819355
hg1919355
hg1819355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787122
Samples
Known GenesTRIM34, TRIM6-TRIM34
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891920
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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