A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6166137



Internal ID9324955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1807027..1811541hg38UCSC Ensembl
Outerchr11:1806990..1811591hg38UCSC Ensembl
Innerchr11:1828257..1832771hg19UCSC Ensembl
Outerchr11:1828220..1832821hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384602
hg194602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663044
Supporting Variants
SamplesNA18519
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6166137
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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