A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3361269



Internal ID15208247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83714203..83714222hg38UCSC Ensembl
Innerchr11:83714199..83714226hg38UCSC Ensembl
Outerchr11:83714180..83714245hg38UCSC Ensembl
chr11:83425246..83425265hg19UCSC Ensembl
Innerchr11:83425242..83425269hg19UCSC Ensembl
Outerchr11:83425223..83425288hg19UCSC Ensembl
chr11:83102894..83102913hg18UCSC Ensembl
Innerchr11:83102917..83102890hg18UCSC Ensembl
Outerchr11:83102871..83102936hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9653213, essv9653202
SamplesNA12814, NA11840
Known GenesDLG2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3361269
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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