A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838981



Internal ID15007894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72420977..72420978hg38UCSC Ensembl
Innerchr11:72420912..72421043hg38UCSC Ensembl
Outerchr11:72420911..72421044hg38UCSC Ensembl
chr11:72132021..72132022hg19UCSC Ensembl
Innerchr11:72131956..72132087hg19UCSC Ensembl
Outerchr11:72131955..72132088hg19UCSC Ensembl
chr11:71809669..71809670hg18UCSC Ensembl
Innerchr11:71809735..71809604hg18UCSC Ensembl
Outerchr11:71809603..71809736hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38142
hg19142
hg18142
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309852
Supporting Variants
SamplesNA19238
Known GenesCLPB
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838981
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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