A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6315632



Internal ID9293035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102397041..102398254hg38UCSC Ensembl
Outerchr11:102397004..102398304hg38UCSC Ensembl
Innerchr11:102267772..102268985hg19UCSC Ensembl
Outerchr11:102267735..102269035hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667796
Supporting Variants
SamplesHG00672
Known GenesTMEM123
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6315632
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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