A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892056



Internal ID18839766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89850051..90041084hg38UCSC Ensembl
Outerchr11:89730855..90168986hg38UCSC Ensembl
Innerchr11:89583219..89774252hg19UCSC Ensembl
Outerchr11:89464023..89902154hg19UCSC Ensembl
Innerchr11:89222867..89413900hg18UCSC Ensembl
Outerchr11:89103671..89541802hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38438132
hg19438132
hg18438132
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778391, essv25791162, essv25791046, essv25790711
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B, UBTFL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892056
Frequency
Sample Size3017
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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