A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6284294



Internal ID9199224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65874145..65876851hg38UCSC Ensembl
Outerchr11:65873774..65877221hg38UCSC Ensembl
Innerchr11:65641616..65644322hg19UCSC Ensembl
Outerchr11:65641245..65644692hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658274
Supporting Variants
SamplesHG01515
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6284294
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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