A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9650924



Internal ID13369584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13070629..13070648hg38UCSC Ensembl
Innerchr11:13070625..13070652hg38UCSC Ensembl
Outerchr11:13070606..13070671hg38UCSC Ensembl
chr11:13092176..13092195hg19UCSC Ensembl
Innerchr11:13092172..13092199hg19UCSC Ensembl
Outerchr11:13092153..13092218hg19UCSC Ensembl
chr11:13048752..13048771hg18UCSC Ensembl
Innerchr11:13048775..13048748hg18UCSC Ensembl
Outerchr11:13048729..13048794hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3432976
Supporting Variants
SamplesNA12045
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9650924
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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