A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891912



Internal ID18839622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4268493..4345966hg38UCSC Ensembl
Outerchr11:4240025..4422242hg38UCSC Ensembl
Innerchr11:4289723..4367196hg19UCSC Ensembl
Outerchr11:4261255..4443472hg19UCSC Ensembl
Innerchr11:4246299..4323772hg18UCSC Ensembl
Outerchr11:4217831..4400048hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38182218
hg19182218
hg18182218
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791178, essv25798652, essv25783515, essv25792776, essv25800716, essv25798177, essv25792756, essv25782851
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891912
Frequency
Sample Size3017
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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