A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891969



Internal ID19186365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42427062..42492936hg38UCSC Ensembl
Outerchr11:42422349..42492936hg38UCSC Ensembl
Innerchr11:42448612..42514486hg19UCSC Ensembl
Outerchr11:42443899..42514486hg19UCSC Ensembl
Innerchr11:42405188..42471062hg18UCSC Ensembl
Outerchr11:42400475..42471062hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3870588
hg1970588
hg1870588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790309, essv25788218
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891969
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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