A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6293541



Internal ID9270944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124662271..124669241hg38UCSC Ensembl
Outerchr11:124662234..124669291hg38UCSC Ensembl
Innerchr11:124532167..124539137hg19UCSC Ensembl
Outerchr11:124532130..124539187hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387058
hg197058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678188
Supporting Variants
SamplesNA19467
Known GenesSIAE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6293541
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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