A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6374455



Internal ID8874135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86589095..86590637hg38UCSC Ensembl
Outerchr11:86589053..86590698hg38UCSC Ensembl
Innerchr11:86300137..86301679hg19UCSC Ensembl
Outerchr11:86300095..86301740hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381646
hg191646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662437
Supporting Variants
SamplesHG00326
Known GenesME3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6374455
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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