A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6450899



Internal ID8987987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108209196..108217292hg38UCSC Ensembl
Outerchr11:108209159..108217342hg38UCSC Ensembl
Innerchr11:108079923..108088019hg19UCSC Ensembl
Outerchr11:108079886..108088069hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388184
hg198184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670718
Supporting Variants
SamplesHG00583
Known GenesNPAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6450899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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