A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837337



Internal ID15081573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29463637..29463638hg38UCSC Ensembl
Innerchr11:29463598..29463677hg38UCSC Ensembl
Outerchr11:29463597..29463678hg38UCSC Ensembl
chr11:29485184..29485185hg19UCSC Ensembl
Innerchr11:29485145..29485224hg19UCSC Ensembl
Outerchr11:29485144..29485225hg19UCSC Ensembl
chr11:29441760..29441761hg18UCSC Ensembl
Innerchr11:29441800..29441721hg18UCSC Ensembl
Outerchr11:29441720..29441801hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381144
hg191144
hg181144
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309368
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837337
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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