A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6311309



Internal ID8790401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119243299..119245574hg38UCSC Ensembl
Outerchr11:119243113..119245775hg38UCSC Ensembl
Innerchr11:119114009..119116284hg19UCSC Ensembl
Outerchr11:119113823..119116485hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665710
Supporting Variants
SamplesHG00232
Known GenesCBL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6311309
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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