A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892067



Internal ID19186463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93101673..93135104hg38UCSC Ensembl
Outerchr11:93100309..93135104hg38UCSC Ensembl
Innerchr11:92834839..92868270hg19UCSC Ensembl
Outerchr11:92833475..92868270hg19UCSC Ensembl
Innerchr11:92474487..92507918hg18UCSC Ensembl
Outerchr11:92473123..92507918hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3834796
hg1934796
hg1834796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787996, essv25787904, essv25788285
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892067
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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