A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432045



Internal ID15279001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112652114..112652131hg38UCSC Ensembl
Innerchr11:112652085..112652160hg38UCSC Ensembl
Outerchr11:112652068..112652177hg38UCSC Ensembl
chr11:112522837..112522854hg19UCSC Ensembl
Innerchr11:112522808..112522883hg19UCSC Ensembl
Outerchr11:112522791..112522900hg19UCSC Ensembl
chr11:112028047..112028064hg18UCSC Ensembl
Innerchr11:112028093..112028018hg18UCSC Ensembl
Outerchr11:112028001..112028110hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865522
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432045
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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