A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6354009



Internal ID9331412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126291589..126292459hg38UCSC Ensembl
Outerchr11:126291422..126292654hg38UCSC Ensembl
Innerchr11:126161484..126162354hg19UCSC Ensembl
Outerchr11:126161317..126162549hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664251
Supporting Variants
SamplesNA20334
Known GenesTIRAP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6354009
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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