A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3323165



Internal ID15170139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:135072448..135076044hg38UCSC Ensembl
Innerchr11:135073448..135075044hg38UCSC Ensembl
Outerchr11:135071448..135076622hg38UCSC Ensembl
chr11:134942342..134945938hg19UCSC Ensembl
Innerchr11:134943342..134944938hg19UCSC Ensembl
Outerchr11:134941342..134946516hg19UCSC Ensembl
chr11:134447552..134451150hg18UCSC Ensembl
Innerchr11:134448552..134450150hg18UCSC Ensembl
Outerchr11:134446552..134452150hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383597
hg193597
hg183599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688225
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3323165
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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